RECA UBEREX

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  • RECA UBEREX
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Lokalizacija

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  • RECA UBEREX
    Hrvatska
  • Jezik:
  • hrvatski

Druge informacije

Status

  • Izvor:
  • Ecolab
  • Broj odobrenja:
  • 113971E
  • Zadnje ažuriranje:
  • 12-03-2018

Sažetak Opisa Svojstava

RECA UBEREX

SIGURNOSNO- TEHNIČKI LIST

Ime proizvoda

RECA UBEREX

Odgovara Regulativi (EC) br. 1907/2006 (REACH), Annex II (453/2010) - Europa

:

1.1 Identifikator proizvoda

1.3 Podaci o dobavljaču koji isporučuje sigurnosno tehnički list

1.2 Odgovarajuće identificirane namjene tvari ili smjese i namjene koje se ne preporučuju

Identificirane uporabe

ODJELJAK 1: Identifikacija tvari/smjese i podaci o tvrtki/poduzeću

Kod proizvoda

:

Ne preporučive uporabe

1.4 Telefon zа hitne slučajeve

Služba za izvanredna stanja

Njega životinja - manulani postupak

Sredstvo za održavanja prostora kućnih ljubimaca. Polu-automatski proces.

Nisu poznati.

Ecolab d.o.o.

Zavrtnica 17

10 000 Zagreb

tel: +385 1 6321 600

fax: +385 1 6321 633

email:iva.nola@ecolab.com

:

Proizvođač/ Distributer/

Uvoznik

:

Broj telefona

Tel.: 112

113971E

Uporaba proizvoda

:

Sredstvo za tretiranje vimena

Ljekoviti proizvod

Samo za profesionalnu uporabu

Medicinske informacije

:

Broj telefona

+385 (0)1 2348 342

Izdanje

: 2

Razvrstavanje

Nije klasificirano

:

:

Druge opasnosti koje ne

rezultiraju u klasifikaciji

Vidjeti odjeljak 11 za detaljnije informacije o utjecajima na zdravlje i mogućim simptomima.

Razvrstavanje prema Uredbi 1999/45/EZ [DPD]

ODJELJAK 2: Identifikacija opasnosti

2.1 Razvrstavanje tvari ili smjese

Definicija proizvoda

:

Smjesa

Vidjeti Odjeljak 16 za cijeli tekst R, H i EUH oznaka.

Razvrstavanje prema Uredbi 1999/45/EZ [DPD]

2.2 Elemenati označavanja prema direktivi 1999/45/EZ ili uredbi (EZ-a) br. 1272/2008 (CLP)

Izjava opasnosti

:

Izjava opreza

2.3 Druge opasnosti

Nije klasificirano

Nema.

Značajne posljedice ili kritične opasnosti nisu poznate.

Datum izdanja/Datum revizije

:

1/10

2 siječnja 2013

HZTA

:

Nema.

RECA UBEREX

Nadzor nad izloženošću, ako je dostupno navedeno je u odjeljku 8.

Ne postoje dodatni sastojci koji su, u okviru sadašnjeg znanja dobavljača i u primjenljivim koncentracijama, klasificirani

opasnim po zdravlje ili okoliš i stoga zahtijevaju podnošenje izvještaja u ovom odjeljku.

ODJELJAK 3: Sastav/informacije o sastojcima

[1] Supstance koje su klasificirane kao opasne za zdravlje ili okolinu

[2] Supstance koje imaju zadanu granicu izlaganja na radnom mjestu

[3] Tvar ispunjava kriterije za PBT prema Propisu (EZ) Br 1207/2006, Aneks XIII

[4] Tvar ispunjava kriterije za vPvB prema Propisu (EZ) Br 1207/2006, Aneks XIII

Br. po REACH-u

EC/CAS/Indeks

67/548/EEC

Naziv

proizvoda/sastojka

%

Tip

Pravilo (EC) Br.

1272/2008 [CLP]

Razvrstavanje

Vidjeti odjeljak 16 za

cijeli tekst R-oznaka

gore deklariranih

Vidjeti Odjeljak 16 za

cijeli tekst H-oznaka

gore deklariranih

EC: 242-354-0

CAS: 18472-51-0

<1

Xi; R41

N; R50

Eye Dam. 1, H318

Aquatic Acute 1, H400

Mješavine

3.2

Isprati usta vodom. Ukoliko je izložena osoba pri svijesti, dati popiti male količine

vode. Ne izazivati povraćanje osim ako to nije naloženo od strane medicinskog

osoblja. Treba primiti liječničku pomoć ukoliko se dogode simptomi.

Kontakt s kožom

Odmah isprati oči s velikom količinom vode, te povremeno podići gornje i donje

kapke. Provjeriti postojanje leća te iste ukloniti. Treba primiti liječničku pomoć

ukoliko dođe do iritacije.

Isprati kontaminiranu kožu s puno vode. Skinuti kontaminiranu odjeću i cipele.

Treba primiti liječničku pomoć ukoliko se dogode simptomi.

4.1 Opis mjera prve pomoći

Premjestiti unesrećenog na svježi zrak, umiriti ga i postaviti u položaj koji olakšava

disanje. Treba primiti liječničku pomoć ukoliko se dogode simptomi.

Obavijesti liječniku

Tretirati po simptomima. Kontaktirati liječnika specijalistu za otrove odmah ukoliko je

osoba progutala ili udisala velike količine.

Gutanje

Udisanje

Kontakt očima

:

:

:

:

:

Zaštita pružaoca prve

pomoći

:

ODJELJAK 4: Mjere prve pomoći

4.2 Najvažniji simptomi i efekti, i akutni i odloženi

Potencijalne akutne zdravstvene posljedice

Udisanje

:

Značajne posljedice ili kritične opasnosti nisu poznate.

Značajne posljedice ili kritične opasnosti nisu poznate.

:

Gutanje

Kontakt s kožom

:

Značajne posljedice ili kritične opasnosti nisu poznate.

Značajne posljedice ili kritične opasnosti nisu poznate.

:

Kontakt očima

Znaci/simptomi pretjeranog izlaganja

Kontakt s kožom

Gutanje

Udisanje

Nema specifičnih podataka.

Nema specifičnih podataka.

Nema specifičnih podataka.

:

:

:

Kontakt očima

:

Nema specifičnih podataka.

4.3 Indikacija potrebe za liječničkom pomoći bez odgode i specijalnim liječenjem

Ne poduzimati ni jednu aktivnost koja uključuje osobni rizik niti aktivnost za koju

osoba nije prošla odgovarajuću obuku.

Datum izdanja/Datum revizije

:

2/10

2 siječnja 2013

HZTA

:

Nema.

RECA UBEREX

ODJELJAK 4: Mjere prve pomoći

Dodatna upozorenja

Nema specifičnog liječenja.

:

U slučaju požara odmah izolirati mjesto događaja uklanjanjem svih osoba koje se

nalaze u blizini. Ne poduzimati ni jednu aktivnost koja uključuje osobni rizik niti

aktivnost za koju osoba nije prošla odgovarajuću obuku.

Opasni samozapaljivi

proizvodi

Opasnosti od tvari ili

smjese

Produkti raspadanja mogu uključivati sljedeće materijale:

ugljikov dioksid

ugljiikov monoksid

U slučaju požara ili ako grijano, dogoditi će se porast tlaka i posuda može prsnuti.

Vatrogasci bi trebali nositi odgovarajuću zaštitnu opremu i samostalni aparat za

disanje koji pokriva čitavo lice i koji je pod pozitivnim tlakom.

Posebna oprema za zaštitu

vatrogasaca

***In case of fire, use water spray (fog), foam, dry chemical, or CO

.***

5.1 Sredstva za gašenje požara

:

:

:

Nisu poznati.

Odgovarajuća sredstva za

gašenje

:

Neodgovarajuća sredstva

za gašenje

:

ODJELJAK 5: Mjere za suzbijanje požara

5.2 Specijalne opasnosti koje proističu od tvari ili smjese

5.3 Savjet za vatrogasce

Specijalna mjere

predostrožnosti za

vatrogasce

:

6.2 Mjere zaštite okoliša

Zaustaviti propuštanje ako ne postoji rizik. Ukloniti spremnike s mjesta izlijevanja.

Spriječiti prilaz kanalizaciji, vodotocima, podrumima ili zatvorenim prostorima. Isprati

izljevanja u postrojenje za prečišćavanje otpadnih voda ili postupiti po slijedećem.

Zadržati i pokupiti izljev negorivim, apsorbirajućim materijalom na pr. pijeskom,

zemljom, vermikulitom, diatomejskom zemljom i smjestiti u kontejner za odlaganje u

skladu s lokalnim pravilima.

Izbjegavati rasipanje prosutog materijala i otjecanje ili kontakt sa tlom, vodotocima,

odvodima i kanalizacijom. Obavijestiti odgovarajuće vlasti ukoliko je proizvod

prouzročio zagađenje okoliša (kanalizacije, vodotokova, tla ili zraka).

Veliko izlijevanje

:

Zaustaviti propuštanje ako ne postoji rizik. Ukloniti spremnike s mjesta izlijevanja.

Razrijediti vodom i prebrisati ako je topivo u vodi. Alternativno, ili ako nije topivo u

vodi, absorbirati sa inertnim suhim materijalom i odložiti u odgovarajući kontejner za

odlaganje otpada.

Malo izlijevanje

:

6.3 Metode i materijali za zadržavanje i čišćenje

ODJELJAK 6: Mjere kod slučajnog ispuštanja

6.1 Osobne mjere predostrožnosti, zaštitna oprema i postupci u slučaju hitnih slučajeva

Za ne-interventno osoblje

:

Za interventno osoblje

:

Ne poduzimati ni jednu aktivnost koja uključuje osobni rizik niti aktivnost za koju

osoba nije prošla odgovarajuću obuku. Spriječiti ulazak nepotrebnog i nezaštićenog

osoblja. Izbjegavati diranje i hodanje po prolivenom materijalu. Staviti prikladnu

osobnu zaštitnu opremu.

Ako je specijalizirana odjeća potrebna za rješavanje izlijevanja, treba obratiti pažnju

na bilo kakve informacije u Odjeljku 8 o prikladnim i neprikladnim materijalima.

Pogledati također informacije u "Za ne-interventno osoblje".

:

Datum izdanja/Datum revizije

:

3/10

2 siječnja 2013

HZTA

:

Nema.

RECA UBEREX

ODJELJAK 6: Mjere kod slučajnog ispuštanja

6.4 Upućivanje na druge

odjeljke

Vidjeti Odjeljak 1 za konakt za hitne informacije.

Vidjeti Odjeljak 8 za informacije o prikladnoj osobnoj zaštitnoj opremi.

Vidjeti Odjeljak 13 za dodatne informacije o obradi otpada.

:

Skladištiti na temperaturi između: 15 do 25°C (59 do 77°F). Skladištiti u skladu sa

lokalnim uredbama. Skladištiti u originalnom spremniku zaštićeno od izravnog

sunčevog svjetla, u suhom, hladnom i dobro ventiliranom prostoru, daleko od

nekompatiblinih materijala (vidjeti odjeljak 10), te hrane i pića. Držati spremnik

čvrsto zatvoren i zapečaćen dok nije spreman za uporabu. Posude koje su otvorene

moraju biti pažljivo nanovo zabrtvljene i držane uspravno radi sprječavanja

odlijevanja. Ne skladištiti u neobilježenim kontejnerima. Koristiti odgovarajuću

ambalažu kako bi se spriječilo zagađivanje okoliša.

ODJELJAK 7: Rukovanje i skladištenje

Informacije u ovom odjeljku sadrže opće savjete i smjernice. Popis identificiranih uporaba u Odjeljku 1 bi se trebao

proučiti za bilo koje dostupno korištenje specifičnih informacija u Scenariju(ima) izloženosti.

7.1 Mjere predostrožnosti za sigurno rukovanje

Sigurnosne mjere

:

Savjet o općoj

profesionalnoj higijeni

:

7.2 Uvjeti za sigurno

skladištenje, uključujući bilo

koje nekompatibilnosti

7.3 Specifični krajnji korisnik(ci)

Staviti odgovarajuću osobnu zaštitnu opremu (vidjeti odjeljak 8).

Radnici trebaju oprati ruke i lice prije jedenja, pijenja i pušenja. Vidjeti također

Odjeljak 8 za dodatne informacije o higijenskim mjerama.

:

Preporuke

:

Specifične otopine za

industrijski sektor

:

Nije primjenjivo dok scenarij izloženosti za tvari ne bude dostupan.

Nije primjenjivo dok scenarij izloženosti za tvari ne bude dostupan.

Odgovarajuće inženjerske

kontrole

:

Nema posebnih ventilacijskih zahtjeva. Dobra opća ventilacija bi trebala biti

dostatna za kontrolu razine čestica prenosivih zrakom kod radnika. Ukoliko ovaj

proizvod sadrži sastojke ograničenog vremena izlaganja, upotrebiti procesne

zatvorene prostore, lokalnu ventilaciju ispušnih plinova ili druge mehaničke

upravljačke uredjaje radi očuvanja izlaganja radnika ispod preporučenih ili

zakonskih limita.

Temeljito oprati ruke, podlaktice i lice nakon rukovanja kemijskim proizvodima, prije

jela, pušenja ili korištenja toaleta te po svršetku radnog vremena. Odgovarajuće

tehnike trebaju biti korištene pri uklanjanju potencijalno kontaminirane odjeće.

Oprati kontaminiranu odjeću prije ponovne upotrebe. Osigurati da su mjesta za

ispiranje očiju i tuševi blizu radnih mjesta.

8.2 Tehničke mjere za smanjenje izloženosti

Higijenske mjere

:

DNEL nije primjenjivo za smjese.

PNEC

PNEC nije primjenjivo za smjese.

ODJELJAK 8: Nadzor nad izloženošću/osobna zaštita

8.1 Kontrolni parametri

DNEL

Individualne mjere zaštite

Naziv proizvoda/sastojka

Granične vrijednosti izloženosti

Limit profesionalnog izlaganja

Nije poznata vrijednost granice izlaganja.

Datum izdanja/Datum revizije

:

4/10

2 siječnja 2013

HZTA

:

Nema.

RECA UBEREX

ODJELJAK 8: Nadzor nad izloženošću/osobna zaštita

Zaštita ruku

(HRN EN 374)

Nema posebnih preporuka.

Nema posebnih preporuka.

Nema posebnih preporuka.

Zaštita оčiju/lica

(HRN EN 166)

Zaštita dišnih puteva

(HRN EN 143, 14387)

:

:

:

Zaštita kože

Nema posebnih preporuka.

:

Kontrole izlaganja zaštite

okoliša

:

Emisije iz ventilacije ili opreme radnog procesa trebaju biti prekontrolirane radi

osiguranja da udovoljavaju zahtjevima zakonskih propisa o ekološkoj zaštiti. U

nekim slučajevima, čistači plina, filteri ili inženjerske preinake procesne opreme biti

će neophodne za redukciju emisija na prihvatljive nivoe.

Zaštita tijela

(HRN EN 14605)

:

Druga zaštita kože

(HRN EN 13832)

Termičke opasnosti

:

Nema posebnih preporuka.

Nema.

ODJELJAK 9: Fizikalna i kemijska svojstva

Agregatno stanje

Talište

Vrelište

Tlak pare

Relativna gustoča

Gustoća pare

Topljivost(i)

Tekućina.

1.011 do 1.015

Lako topivo u slijedećim materijalima: hladnoj vodi i topla vodi.

Bez mirisa.

Miris

pH

Zelen.

Boja

Brzina isparavanja

Temperatura samozapaljena

Plamište

> 100°C

6 do 6.6 [Konc. (% t/t): 100%]

Prag mirisa:

Oktanol/voda koeficijent

raspodjele

Eksplozivnost

:

:

:

:

:

:

:

:

:

:

:

:

:

:

:

:

Ne postoji.

Oksidativnost

:

9.1 Informacije o osnovnim fizikalnim i kemijskim svojstvima

Izgled

9.2 Ostale informacije

Vrijeme izgaranja

Brzina izgaranja

:

:

Temperatura dekompozicije

:

Ne može se primijeniti i /ili odrediti iz mješavine.

Ne može se primijeniti i /ili odrediti iz mješavine.

Ne može se primijeniti i /ili odrediti iz mješavine.

Ne može se primijeniti i /ili odrediti iz mješavine.

Ne može se primijeniti i /ili odrediti iz mješavine.

Ne može se primijeniti i /ili odrediti iz mješavine.

Ne može se primijeniti i /ili odrediti iz mješavine.

Ne može se primijeniti i /ili odrediti iz mješavine.

Ne može se primijeniti i /ili odrediti iz mješavine.

Ne može se primijeniti i /ili odrediti iz mješavine.

Ne može se primijeniti i /ili odrediti iz mješavine.

Nema.

Ne može se primijeniti i /ili odrediti iz mješavine.

Viskozitet

:

Gornje/donje granice

zapaljivosti ili eksplozivnosti

:

Ne može se primijeniti i /ili odrediti iz mješavine.

Zapaljivost (krutina, plin)

:

Ne može se primijeniti i /ili odrediti iz mješavine.

Datum izdanja/Datum revizije

:

5/10

2 siječnja 2013

HZTA

:

Nema.

RECA UBEREX

ODJELJAK 9: Fizikalna i kemijska svojstva

Nema dodatnih informacija.

10.6 Opasni proizvodi

raspadanja

10.4 Uvjeti koje treba

izbjegavati

Nema specifičnih podataka.

Pod normalnim uvjetima skladištenja i uporabe, opasni proizvodi raspadanja ne bi

smjeli biti proizvedeni.

Proizvod je stabilan.

10.2 Kemijska stabilnost

:

:

:

10.3 Mogućnost opasnih

reakcija

:

Pod normalnim uvjetima skladištenja i uporabe, opasne reakcije se neće dogoditi.

ODJELJAK 10: Stabilnost i reaktivnost

10.1 Reaktivnost

:

Na raspolaganju nema specifičnih test podataka vezanih za reaktivnost za ovaj

proizvod ili njegove sastojke.

10.5 Nekompatibilni

materijali

:

Nema specifičnih podataka.

akutno trovanje

LD50 Oralno

Štakor

2 g/kg

LD50 Oralno

Štakor

2040 mg/kg

Naziv proizvoda/sastojka

Rezultat

Vrste

Doza

Izlaganje

Karcinogenost

Mutagenost

Teratogenost

Reproduktivna toksičnost

Iritacija/korozija

Zaključak/Sažetak

:

Značajne posljedice ili kritične opasnosti nisu poznate.

Preosjetljivost

Zaključak/Sažetak

:

Značajne posljedice ili kritične opasnosti nisu poznate.

ODJELJAK 11: Toksikološke informacije

11.1 Informacije o toksikološkim učincima

Akutne procjene toksičnosti

Nema podataka za proizvod.

Toksičnost specifično određenih organa (samo jedno izlaganje)

Toksičnost specifično određenih organa (ponovljeno izlaganje)

Opasnost od aspiracije

Značajne posljedice ili kritične opasnosti nisu poznate.

Značajne posljedice ili kritične opasnosti nisu poznate.

Zaključak/Sažetak

:

Značajne posljedice ili kritične opasnosti nisu poznate.

Zaključak/Sažetak

:

Značajne posljedice ili kritične opasnosti nisu poznate.

Zaključak/Sažetak

:

Značajne posljedice ili kritične opasnosti nisu poznate.

Zaključak/Sažetak

:

Značajne posljedice ili kritične opasnosti nisu poznate.

Zaključak/Sažetak

:

Značajne posljedice ili kritične opasnosti nisu poznate.

Datum izdanja/Datum revizije

:

6/10

2 siječnja 2013

HZTA

:

Nema.

RECA UBEREX

ODJELJAK 11: Toksikološke informacije

Potencijalne kronične zdravstvene posljedice

Potencijalne akutne zdravstvene posljedice

Udisanje

:

Značajne posljedice ili kritične opasnosti nisu poznate.

Značajne posljedice ili kritične opasnosti nisu poznate.

:

Gutanje

Kontakt s kožom

:

Značajne posljedice ili kritične opasnosti nisu poznate.

Značajne posljedice ili kritične opasnosti nisu poznate.

:

Kontakt očima

Značajne posljedice ili kritične opasnosti nisu poznate.

Opća

:

Značajne posljedice ili kritične opasnosti nisu poznate.

Karcinogenost

:

Značajne posljedice ili kritične opasnosti nisu poznate.

Mutagenost

:

Značajne posljedice ili kritične opasnosti nisu poznate.

Teratogenost

:

Razvojni efekti

:

Značajne posljedice ili kritične opasnosti nisu poznate.

Efekti fertilnosti

:

Značajne posljedice ili kritične opasnosti nisu poznate.

Simptomi u svezi s fizičkim, kemijskim i toksikološkim karakteristikama

Kontakt s kožom

Gutanje

Udisanje

Nema specifičnih podataka.

Nema specifičnih podataka.

Nema specifičnih podataka.

:

:

:

Kontakt očima

:

Nema specifičnih podataka.

Efekti sa i bez odgode te također kronični efekti od kratkotrajnog i dugotrajnog izlaganja

Kratkotrajno izlaganje

Dugotrajno izlaganje

Značajne posljedice ili kritične opasnosti nisu poznate.

Informacije o vjerojatnim

putevima izlaganja

:

Značajne posljedice ili kritične opasnosti nisu poznate.

Potencijalni neposredni

učinci

:

Potencijalni odgođeni

učinci

:

Potencijalni neposredni

učinci

:

Potencijalni odgođeni

učinci

:

Značajne posljedice ili kritične opasnosti nisu poznate.

Značajne posljedice ili kritične opasnosti nisu poznate.

Značajne posljedice ili kritične opasnosti nisu poznate.

Značajne posljedice ili kritične opasnosti nisu poznate.

Zaključak/Sažetak

:

Značajne posljedice ili kritične opasnosti nisu poznate.

Ostale informacije

:

Značajne posljedice ili kritične opasnosti nisu poznate.

ODJELJAK 12: Ekološke informacije

12.1 Otrovnost

Akutni EC50 0.05 do 0.1 mg/L

Vodenbuha

48 sati

Akutni IC50 0.011 mg/L

Alge

72 sati

Akutni LC50 10.4 mg/L

Riba

96 sati

Naziv proizvoda/sastojka

Vrste

Rezultat

Izlaganje

12.2 Postojanost i razgradivost

Zaključak/Sažetak

:

Sve organske substance sadržane u proizvodu dostižu >60% BOD/COD ili CO2

otpuštanje, ili >70% DOC redukciju u testovima lakše razgradljivosti - granične

vrijednosti za "readily" razgradljivost (prema OECD metodi 301)

Zaključak/Sažetak

:

Značajne posljedice ili kritične opasnosti nisu poznate.

Datum izdanja/Datum revizije

:

7/10

2 siječnja 2013

HZTA

:

Nema.

RECA UBEREX

ODJELJAK 12: Ekološke informacije

12.3 Bioakumulativni potencijal

12.6 Drugi štetni efekti

Značajne posljedice ili kritične opasnosti nisu poznate.

PBT

:

Nema.

vPvB

:

Nema.

12.4 Pokretljivost kroz tlo

12.5 Rezultati OBT i vPvB procjene

:

Tlo/voda koeficijent

raspodjele (K

OC

)

:

Nema podataka za proizvod.

Pokretljivost

:

Nema podataka za proizvod.

Zaključak/Sažetak

:

Nema podataka za proizvod.

Katalog Europskog otpada (EWC)

U okviru sadašnjeg znanja dobavljača, ovaj proizvod se ne smatra opasnim

otpadom, kao što je definirano EU Uredbom 91/689/EEC.

Opasni otpad

:

Stvaranje otpada treba izbjegavati ili umanjiti gdje god je to moguće. Prazni

kontejneri ili cijevi mogu zadržati nešto ostatka proizvoda. Ostaci tvari i spremnici

moraju biti odloženi na siguran način. Značajne količine otpadnog ostatka proizvoda

ne bi trebale biti odložene putem kanalizacije, nego procesirane u odgovarajućem

pogonu za obradu otpadne vode. Ukloniti suvišak i ne-reciklirajuće proizvode preko

ovlaštene osobe za odlaganje otpada. Odlaganje ovog proizvoda, otopine i bilo

kojeg nus proizvoda mora uvijek biti u skladu sa zahtjevima zaštite okoliša i

zakonima o odlaganju otpada i bilo kojim regionalnim zahtjevima lokalne uprave.

Izbjegavati rasipanje prosutog materijala i otjecanje ili kontakt sa tlom, vodotocima,

odvodima i kanalizacijom.

:

Metode odlaganja

ODJELJAK 13: Zbrinjavanje

Informacije u ovom odjeljku sadrže opće savjete i smjernice. Popis identificiranih uporaba u Odjeljku 1 bi se trebao

proučiti za bilo koje dostupno korištenje specifičnih informacija u Scenariju(ima) izloženosti.

13.1 Metode prerade otpada

Proizvod

Pakiranje

Kod otpada

Oznaka otpada

Metode odlaganja

:

Specijalne mjere

predostrožnosti

:

20 01 30

deterdženti koji nisu navedeni pod 20 01 29

Stvaranje otpada treba izbjegavati ili umanjiti gdje god je to moguće. Ambalažni

otpad treba biti recikliran.

Ostaci tvari i spremnici moraju biti odloženi na siguran način. Prazni kontejneri ili

cijevi mogu zadržati nešto ostatka proizvoda. Izbjegavati rasipanje prosutog

materijala i otjecanje ili kontakt sa tlom, vodotocima, odvodima i kanalizacijom.

ODJELJAK 14: Informacije o prijevozu

Datum izdanja/Datum revizije

:

8/10

2 siječnja 2013

HZTA

:

Nema.

RECA UBEREX

ODJELJAK 14: Informacije o prijevozu

Not regulated.

Nije regulirano

Nije regulirano

Not regulated.

ADR/RID

IMDG

IATA

14.1 UN broj

14.2 UN ispravni

otpremni naziv

14.3 Klasa(e)

opasnosti pri

transportu

14.4 Ambalažna

skupina

ADN/ADNR

14.5 Opasnosti za

okoliš

14.6 Specijalna

mjere

predostrožnosti za

korisnika

14.7 Transport u

nezapakiranom stanju

prema Aneks II MARPOL

73/78 i IBC Kodu

:

Nema.

Ne postoji.

Ne postoji.

None.

None.

Nacionalna regulativa

Ostala EU pravila

Nema.

Aneks XVII – Restrikcija

na proizvodnju, stavljanje

na tržište i uporabu

određenih opasnih tvari,

smjesa i artikala

:

Hrvatska

ODJELJAK 15: Informacije o propisima

15.1 Pravila/zakonski propisi o sigurnosti, zdravlju i zaštiti okoliša, specifični za tvar ili smjesu

EU Pravilo (EC) Br 1907/2006 (REACH)

Aneks XIV – Lista tvari podvrgnutih odobrenju

Supstance vrlo visoke zabrinutosti

Ni jedna komponenta nije izlistana.

Zakon o kemikalijama, Pravilnik o razvrstavanju, označavanju, obilježavanju i pakiranju opasnih kemikalija-rađen

prema DSD i DPD direktivama, Pravilnik o razvrstavanju, označavanju, obilježavanju i pakiranju opasnih kemikalija-

rađen prema CLP-u Zakon o biocidnim pripravcima , Pravilniku o dokumentaciji za ocjenu aktivne tvari u biocidnim

pripravcima, dokumentaciji za ocjenu biocidnih pripravaka, postupcima ocjenjivanja biocidnih pripravaka i njihove

uporabe te o vrstama biocidnih pripravaka s njihovim opisima i jedinstvenim načelima za ocjenjivanje biocidnih

pripravaka, Pravilniku o popisu aktivnih tvari u biocidnim pripravcima, Pravilniku o popisu postojećih aktivnih tvari

dopuštenih u biocidnim pripravcima, Pravilniku o popisu postojećih aktivnih tvari koje nisu dopuštene u biocidnim

pripravcima, Pravilniku o ispunjavanja Sigurnosno-tehničkog lista , Pravilnik o graničnim vrijednostima izloženosti

opasnim tvarima pri radu i o biološkim graničnim vrijednostima, Zakon o zaštiti na radu, Zakon o prijevozu opasnih

tvari, Pravilnik o deterdžentima.

Datum izdanja/Datum revizije

:

9/10

2 siječnja 2013

HZTA

:

Nema.

RECA UBEREX

ODJELJAK 15: Informacije o propisima

15.2 Procjena sigurnosti

kemikalije

Nema.

:

2 siječnja 2013

Datum tiskanja

Datum izdanja/ Datum

revizije

Izdanje

Informacije navedene u ovom dokumentu smatraju se vjerodostojnima s obzirom na pravila korištena u

proizvodnji sredstava u zemlji porijekla.

Napomena

Datum prethodnog izdanja

:

:

:

:

Naznačuje informacije koje su se promijenile od prethodne izdane verzije.

2 siječnja 2013

Nema prethodnih validacija

ODJELJAK 16: Ostale informacije

Kratice i akronimi

:

ADN/ADNR = European Provisions concerning the International Carriage of

Dangerous Goods by Inland Waterway

ADR = Europski sporazum u vezi s internacionalnim prijevozom opasne robe cestom

ATE- Procijenjene vrijednosti akutne toksičnosti.

BKF = Biokoncentracijski faktor

CLP- Uredba o razvrstavanju, označavanju i pakiranju kemijskih tvari i mješavina

(regulativa (EU) br. 1272/2008

DNEL - Izvedena razina izloženosti bez učinka

DPD = Direktiva o opasnim pripravcima [1999/45/EZ]

EC = Europska Komisija

EUH izjava - CLP Ddopunske oznake upozorenja

IATA = Internacionalno udruženje zračnog transporta

IBC = Kontejner srednjeg obujma

IMDG = Internacionalne pomorski opasne tvari

LogPow = logaritam koeficijenta razdjeljenja između oktanola i vode

MARPOL 73/78 = Internacionalna konvencija za prevenciju zagađivanja od brodova,

1973 modificirano protokolom iz 1978. ("Marpol" = zagađenje mora)

OEL = Profesionalna granica izloženosti

PBT = Postojan, bioakumulativni i toksični

PNEC - Predviđena koncentracija bez učinka

REACH = Registracija, Evaluacija, Autorizacija i Restrikcija Kemijskih Regulativa

[Uredba (EZ) Br. 1907/2006]

RID = Uredba u vezi internacionalnog prijevoza opasnih tvari željezničkim putem

REACH #- Broj REACH registracije

vPvB = Vrlo otporno i vrlo bioakumulativno

Procedura koja se koristi za dobivanje klasifikacije prema Propisu (EC) Br 1272/2008 [CLP/GHS]

Razvrstavanje

Obrazloženje

Nije klasificirano

Cijeli tekst skraćenih R

oznaka

:

R 41 Opasnost od teških ozljeda očiju

R 50 Vrlo otrovno za organizme koji žive u vodi

:

Cijeli tekst klasifikacija

[DSD/DPD]

Cijeli tekst skraćenih H

iskaza

:

Cijeli tekst klasifikacija

[CLP/GHS]

:

H318

Uzrokuje teške ozljede oka.

H400

Vrlo otrovno za vodeni okoliš.

Aquatic Acute 1, H400

VODENA TOKSIČNOST (AKUTNO) - Kategorija 1

Eye Dam. 1, H318

ozbiljne ozljede očiju/NADRAŽUJE OČI - Kategorija 1

Xi - Nadražajuće

N - Opasno za okoliš

Datum izdanja/Datum revizije

:

10/10

2 siječnja 2013

HZTA

:

Nema.

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FDA - U.S. Food and Drug Administration

19-11-2018

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Health Canada

19-11-2018

Indigo Books & Music Inc. recalls American Girl WellieWishers Magic Theater Play Tent

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Health Canada

19-11-2018

Dollarama recalls MONTOY Doll and Toy Furniture Set

Dollarama recalls MONTOY Doll and Toy Furniture Set

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Health Canada

17-11-2018

The Quaker Oats Company Issues Voluntary Recall of a Small Quantity of Cap’n Crunch’s Peanut Butter Crunch Cereal Distributed to Five Target Stores Due to Possible Health Risk

The Quaker Oats Company Issues Voluntary Recall of a Small Quantity of Cap’n Crunch’s Peanut Butter Crunch Cereal Distributed to Five Target Stores Due to Possible Health Risk

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FDA - U.S. Food and Drug Administration

17-11-2018

Chukar Cherries Issues Allergy Alert on Undeclared Milk in 7.5 Oz Amaretto Rainier Chocolate Cherries Pouches

Chukar Cherries Issues Allergy Alert on Undeclared Milk in 7.5 Oz Amaretto Rainier Chocolate Cherries Pouches

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FDA - U.S. Food and Drug Administration

17-11-2018

Recall of Green Cedar Dairy Ackawi Cheese Bearing a Sell by Date of March 26, 2019 or Later

Recall of Green Cedar Dairy Ackawi Cheese Bearing a Sell by Date of March 26, 2019 or Later

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FDA - U.S. Food and Drug Administration

15-11-2018

Vanpak Limited recalls various Cosmetic products in pressurised containers.

Vanpak Limited recalls various Cosmetic products in pressurised containers.

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Health Canada

15-11-2018

LÍLLÉbaby recalls Active Baby Carriers

LÍLLÉbaby recalls Active Baby Carriers

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Health Canada

15-11-2018

Bouclair Inc. recalls Fabric and Rubberwood Barstools

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Health Canada

15-11-2018

MPS Canada Corporation recalls various Cosmetic products in pressurised containers.

MPS Canada Corporation recalls various Cosmetic products in pressurised containers.

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Health Canada

14-11-2018

Nor Cal Food Solutions, LLC ISSUES ALLERGY ALERT ON UNDECLARED Tree Nut – Walnut in The Purveyors Kitchen - Pumpkin Pesto Tapenade

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FDA - U.S. Food and Drug Administration

14-11-2018

Several children's strawberry-flavoured acetaminophen syrups recalled because of defective child-resistant safety caps on the bottles

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Health Canada

14-11-2018

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Health Canada

13-11-2018

The Pictsweet Company Recalls 8-ounce Steam’ables Asparagus Spears due to Potential for <em>Listeria Monocytogenes</em>

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13-11-2018

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FDA - U.S. Food and Drug Administration

13-11-2018

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FDA - U.S. Food and Drug Administration

10-11-2018

Recall of Bittersweet & Feve Chocolate Bars Due to High Levels of Milk Allergens

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FDA - U.S. Food and Drug Administration

9-11-2018

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FDA - U.S. Food and Drug Administration

9-11-2018

Natural Life Pet Products Expands Recall of Dry Food Due to Elevated Levels of Vitamin D

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FDA - U.S. Food and Drug Administration

9-11-2018

Sandoz Inc. Issues Voluntary Nationwide Recall of One Lot of Losartan Potassium and Hydrochlorothiazide Due to the Detection of Trace Amounts of NDEA (N-Nitrosodiethylamine) Impurity Found in the Active Pharmaceutical Ingredient (API)

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Sandoz Inc. is voluntarily recalling one lot of Losartan Potassium Hydrochlorothiazide Tablets, USP 100mg/25mg to the consumer level. This product is being recalled due to the trace amount of an impurity, N-nitrosodiethylamine (NDEA) contained in the API Losartan, USP manufactured by Zhejiang Huahai Pharmaceutical Co. Ltd. Sandoz Inc. Losartan Potassium Hydrochlorothiazide product is manufactured by Lek Pharmaceuticals dd, Ljubljana, Slovenia. This impurity, which is a substance that occurs naturally in ...

FDA - U.S. Food and Drug Administration

9-11-2018

First Choice Vapor recalls Unflavoured 100 mg Nicotine Base E-Liquids

First Choice Vapor recalls Unflavoured 100 mg Nicotine Base E-Liquids

These vaping products do not meet requirements of the Consumer Chemicals and Containers Regulations, 2001 (CCCR, 2001) under the Canada Consumer Product Safety Act.

Health Canada

9-11-2018

Baked Potatoes with Cheddar Cheese and Bacon (2 Count) Mis-Labeled as Herb Roasted Potatoes

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Ukrop’s Homestyle Foods is voluntarily recalling Baked Potatoes with Cheddar Cheese and Bacon (2 count), as the product is mislabeled Herb Roasted Potatoes (see photo attached).

FDA - U.S. Food and Drug Administration

8-11-2018

Wegmans Food Markets, Inc. Issues Allergy Alert on Undeclared Milk in Wegmans Pumpkin Loaf, 11 oz., and Wegmans Placek Coffee Cake, 11 oz. and 22 oz.

Wegmans Food Markets, Inc. Issues Allergy Alert on Undeclared Milk in Wegmans Pumpkin Loaf, 11 oz., and Wegmans Placek Coffee Cake, 11 oz. and 22 oz.

Wegmans has initiated a voluntary recall of the following products because they may contain milk not declared on the label. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume this product.

FDA - U.S. Food and Drug Administration

7-11-2018

Kadesh Incorporation Issues Voluntary Nationwide Recall of Puriton Eye Relief Drops Due to Non-Sterile Production Conditions

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FDA - U.S. Food and Drug Administration

7-11-2018

Several store-brand pain or sinus relief tablets recalled because consumers may be unable to access important safety information

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Vita Health Products is voluntarily recalling several store-brand (Care, Exact, Life, and Pharmasave) over-the-counter drugs used for pain or sinus relief because of a labelling issue. Consumers may be unable to peel open the wrap-around label on the bottle to access the warning statements, or the label may not peel off completely, which may make it difficult to read some of the important safety information.

Health Canada

7-11-2018

Nature's Ultimate recalls NuWrench and NuStainless Products

Nature's Ultimate recalls NuWrench and NuStainless Products

The recalled products are not provided with the required child-resistant containers required by the Consumer Chemicals and Containers Regulations, 2001 under the Canada Consumer Product Safety Act.

Health Canada

7-11-2018

Murray Wholesale Cash & Carry recalls King Universal Butane Fuel

Murray Wholesale Cash & Carry recalls King Universal Butane Fuel

The recalled products do not have proper hazard labelling as required by the Consumer Chemicals and Containers Regulations, 2001 under the Canada Consumer Product Safety Act.

Health Canada

7-11-2018

Sprout Creek Farm Recalls "Margie" Cheese Due to Listeria Monocytogenes

Sprout Creek Farm Recalls "Margie" Cheese Due to Listeria Monocytogenes

Sprout Creek Farm of Poughkeepsie, New York is recalling 132 wheels of "Margie" cheese, because it has the potential to be contaminated with Listeria monocytogenes. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

FDA - U.S. Food and Drug Administration

6-11-2018

FDA Investigating Recalled Duncan Hines Cake Mixes Potentially Linked to Salmonella Agbeni Illnesses

FDA Investigating Recalled Duncan Hines Cake Mixes Potentially Linked to Salmonella Agbeni Illnesses

The FDA is investigating the manufacturing facility that made recalled Duncan Hines cake mixes.

FDA - U.S. Food and Drug Administration

6-11-2018

Duncan Hines Classic White, Classic Butter Golden, Signature Confetti and Classic Yellow Cake Mixes Recalled Due to Potential Presence of Salmonella

Duncan Hines Classic White, Classic Butter Golden, Signature Confetti and Classic Yellow Cake Mixes Recalled Due to Potential Presence of Salmonella

Conagra Brands is collaborating with health officials in connection with a positive finding of Salmonella in a retail sample of Duncan Hines Classic White cake mix that may be linked to a Salmonella outbreak that is currently being investigated by CDC and FDA. While it has not been definitively concluded that this product is linked to the outbreak and the investigation is still ongoing, Conagra has decided to voluntarily recall the specific Duncan Hines variety identified (Classic White) and three other ...

FDA - U.S. Food and Drug Administration

5-11-2018

Statement from FDA Commissioner Scott Gottlieb, M.D., on FDA’s effort to make more robust use of mandatory recall authority to quickly remove unsafe foods from the market

Statement from FDA Commissioner Scott Gottlieb, M.D., on FDA’s effort to make more robust use of mandatory recall authority to quickly remove unsafe foods from the market

Statement from FDA Commissioner Scott Gottlieb, M.D., on FDA’s effort to make more robust use of mandatory recall authority to quickly remove unsafe foods from the market

FDA - U.S. Food and Drug Administration

5-11-2018

STIHL Limited recalls STIHL MSA 161 T Battery Operated Arborist Chain Saw

STIHL Limited recalls STIHL MSA 161 T Battery Operated Arborist Chain Saw

The side inter-lock button may stick when gripping the machine, which could cause the throttle trigger to remain depressed and the chain to continue to run even after releasing the throttle trigger. This can pose a risk of laceration to the user or bystander.

Health Canada

5-11-2018

Home Hardware Stores Ltd. Recalls Benchmark Step Ladder with Tray

Home Hardware Stores Ltd. Recalls Benchmark Step Ladder with Tray

The platform on the ladder does not lock securely in place posing a potential fall hazard.

Health Canada

5-11-2018

Vanpak Limited recalls David Ross Extra purified Butane gas

Vanpak Limited recalls David Ross Extra purified Butane gas

The recalled products do not have proper hazard labelling as required by the Consumer Chemicals and Containers Regulations, 2001 under the Canada Consumer Product Safety Act. Improper labelling could result in unintentional exposure to these products and lead to serious illness, injury or death.

Health Canada

3-11-2018

Nutrisca Issues Recall of Dry Dog Food Due to Elevated Levels of Vitamin D

Nutrisca Issues Recall of Dry Dog Food Due to Elevated Levels of Vitamin D

Nutrisca, of Saint Louis, Missouri is voluntarily recalling one formula of Nutrisca dry dog food (described below) due to it containing elevated levels of vitamin D.

FDA - U.S. Food and Drug Administration

3-11-2018

Natural Life Pet Products Issues Recall of Dry Food Due to Elevated Levels of Vitamin D

Natural Life Pet Products Issues Recall of Dry Food Due to Elevated Levels of Vitamin D

Natural Life Pet Products of Saint Louis, Missouri is voluntarily recalling our Chicken & Potato dry dog food (described below) due to it containing elevated levels of Vitamin D.

FDA - U.S. Food and Drug Administration

3-11-2018

Janssen Issues Voluntary Nationwide Recall for one lot of ORTHO-NOVUM 1/35 and two lots of ORTHO-NOVUM 7/7/7 Due to Incorrect Veridate Dispenser Instructions

Janssen Issues Voluntary Nationwide Recall for one lot of ORTHO-NOVUM 1/35 and two lots of ORTHO-NOVUM 7/7/7 Due to Incorrect Veridate Dispenser Instructions

Janssen Pharmaceuticals, Inc. has initiated a voluntary recall of one lot of ORTHO-NOVUM 1/35 (norethindrone / ethinyl estradiol) Tablets and two lots of ORTHO-NOVUM 7/7/7 (norethindrone / ethinyl estradiol) Tablets to the pharmacy level. The patient information provided inside affected packages of ORTHO-NOVUM does not include the appropriate instructions for the Veridate dispenser.

FDA - U.S. Food and Drug Administration

2-11-2018

Frito-Lay Issues Allergy Alert on Undeclared Milk In Select Smartfood Delight Sea Salt Flavored Popcorn

Frito-Lay Issues Allergy Alert on Undeclared Milk In Select Smartfood Delight Sea Salt Flavored Popcorn

Frito-Lay announced a voluntary recall of select 1/2 oz. bags of Smartfood Delight Sea Salt Flavored popcorn because they were inadvertently filled with cheese flavored tortilla chips that contain undeclared milk ingredients. The recalled bags were sold only in the two variety packs listed below.

FDA - U.S. Food and Drug Administration

2-11-2018

Barcelona Nut Company Recalls Roasted and Salted in Shell Pistachios Because of Possible Health Risk

Barcelona Nut Company Recalls Roasted and Salted in Shell Pistachios Because of Possible Health Risk

Barcelona Nut Company of Baltimore, Maryland is recalling 239 cases of roasted and salted in shell pistachios, because it has the potential to be contaminated with Salmonella, an organism that can cause serious and sometimes-fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain.

FDA - U.S. Food and Drug Administration

2-11-2018

Brin de Folie recalls Wind-up Racoon Toys

Brin de Folie recalls Wind-up Racoon Toys

Health Canada's sampling and evaluation program has determined that the affected products do not meet the Canadian safety requirements for toys. The tail can detach from the toy, posing a choking hazard to young children.

Health Canada

1-11-2018

FDA warns patients and doctors about risk of inaccurate results from home-use device to monitor blood thinner warfarin

FDA warns patients and doctors about risk of inaccurate results from home-use device to monitor blood thinner warfarin

Roche Diagnostics issued voluntary recall of certain test strips used with CoaguChek meter devices; patients affected by the recall should seek alternative methods for testing.

FDA - U.S. Food and Drug Administration

1-11-2018

Stanley Black & Decker Canada Corp. recalls certain Porter-Cable and Black & Decker hammer drills

Stanley Black & Decker Canada Corp. recalls certain Porter-Cable and Black & Decker hammer drills

The side handle supplied with the drill may slip when the drill is in use and lead to loss of control, posing a risk of injury.

Health Canada

30-10-2018

Sciegen Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Irbesartan Tablets, USP  75 Mg, 150 Mg, and 300 Mg Due to The Detection of Trace Amounts of NDEA (N-Nitrosodiethylamine) Impurity Found in The Active Pharmaceutical Ingredient (API)

Sciegen Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Irbesartan Tablets, USP 75 Mg, 150 Mg, and 300 Mg Due to The Detection of Trace Amounts of NDEA (N-Nitrosodiethylamine) Impurity Found in The Active Pharmaceutical Ingredient (API)

ScieGen Pharmaceuticals, Inc. is voluntarily recalling listed lots, within expiry, of Irbesartan Tablets, USP 75 mg, 150 mg, and 300 mg dosage forms to the consumer level. These products are being recalled due to the presence of an impurity, N-nitrosodiethylamine (NDEA) contained in the API Irbesartan, USP manufactured by Aurobindo Pharma Limited. This impurity, which is a substance that occurs naturally in certain foods, drinking water, air pollution, and industrial processes, has been classified as a...

FDA - U.S. Food and Drug Administration

30-10-2018

Food Recall of Fit & Active Southwest Veggie Stuffed Sandwiches Due to Possible Listeria monocytogenes and Salmonella Contamination in Vegetables

Food Recall of Fit & Active Southwest Veggie Stuffed Sandwiches Due to Possible Listeria monocytogenes and Salmonella Contamination in Vegetables

J&J Snack Foods Handheld Corp. of Holly Ridge, NC is voluntarily recalling two lots of Fit & Active Southwest Veggie Stuffed Sandwiches due to potential contamination with Listeria monocytogenes and Salmonella. Salmonella is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

FDA - U.S. Food and Drug Administration

30-10-2018

Mountain Warehouse Limited recalls BPA-Free Printed Kids' Water Bottles

Mountain Warehouse Limited recalls BPA-Free Printed Kids' Water Bottles

If the spout of the water bottle becomes detached during use, a small ring can be exposed and both the spout and the ring may pose a choking hazard.

Health Canada

29-10-2018

Aurobindo Pharma Limited Issues Voluntary Recall of Irbesartan Drug Substance due to the Detection of Trace Amounts of NDEA (NNitrosodiethylamine) Impurity Found in the Active Pharmaceutical Ingredient (API)

Aurobindo Pharma Limited Issues Voluntary Recall of Irbesartan Drug Substance due to the Detection of Trace Amounts of NDEA (NNitrosodiethylamine) Impurity Found in the Active Pharmaceutical Ingredient (API)

Aurobindo Pharma Limited is voluntarily recalling 22 Batches of the drug substance Irbesartan due to the presence of an impurity, N-nitrosodiethylamine (NDEA). The impurity, which is a substance that occurs naturally in certain foods, drinking water, air pollution, and industrial processes, has been classified as a probable human carcinogen as per International Agency for Research on Cancer (IARC).

FDA - U.S. Food and Drug Administration

29-10-2018

Maribel’s Sweets Inc. Allergy Alert on Undeclared Milk Allergens in Chocolate Bars

Maribel’s Sweets Inc. Allergy Alert on Undeclared Milk Allergens in Chocolate Bars

Maribel’s Sweets Inc. of Brooklyn, NY is recalling its 2.82oz MarieBelle Japanese Matcha Japanese Green Tea and White Chocolate Bar, container code 101619, Cacao Market by MarieBelle Rosemary Truffle Salt 60% Dark Chocolate Bar, all container codes, and the Cacao Market by MarieBelle Orange Peels 60% Dark Chocolate Bar, all container codes, because they may contain undeclared milk allergens. Consumers who are allergic to milk allergens may run the risk of serious or life-threatening allergic reactions if...

FDA - U.S. Food and Drug Administration

26-10-2018

Urgent: Curry Spice Recall

Urgent: Curry Spice Recall

This voluntary recall has been initiated by UBC Food Distributors Inc, due to a high level of lead found in the product after testing was done by the Michigan Department of Agriculture & Rural Development, which found high traces of lead.

FDA - U.S. Food and Drug Administration

25-10-2018

i play., inc. recalls Flower Rattle

i play., inc. recalls Flower Rattle

Pieces of the rattle can detach, posing a choking hazard to infants.

Health Canada

25-10-2018

CB2 recalls Colby Lacquered Wood and Glass Ceiling Pendant Light

CB2 recalls Colby Lacquered Wood and Glass Ceiling Pendant Light

The insulation on the electrical wiring may come loose, posing a fire and shock hazard.

Health Canada

25-10-2018

BLL Enterprises Inc. recalls Fluid Film Rust & Corrosion Protection Aerosol

BLL Enterprises Inc. recalls Fluid Film Rust & Corrosion Protection Aerosol

The recalled products do not have proper hazard labelling required by the Consumer Chemicals and Containers Regulations, 2001 under the Canada Consumer Product Safety Act.

Health Canada

25-10-2018

Shirley’s Cookie Company In. Issues Allergy Alert on Undeclared Peanuts in "Chocolate Whoopie Pie"

Shirley’s Cookie Company In. Issues Allergy Alert on Undeclared Peanuts in "Chocolate Whoopie Pie"

Shirley’s Cookie Company Inc. of Claysburg, PA, is recalling its 16 ounce packages of "Chocolate Whoopie Pie" because they may contain undeclared peanuts. People who have allergies to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.

FDA - U.S. Food and Drug Administration

24-10-2018

Sirob Imports, Inc. Issues Recall Due to Elevated Lead in Spices

Sirob Imports, Inc. Issues Recall Due to Elevated Lead in Spices

Sirob Imports, Inc of Lindenhurst, NY is recalling, Corrado, Orlando Imports, Nouri’s Syrian Bakery, Mediterranean Specialty Foods Brand and Butera Fruit Market Curry Powder because it contains elevated levels of lead.

FDA - U.S. Food and Drug Administration

24-10-2018

G & C Raw, LLC is Expanding Recall to Include All Product Lots Manufactured from February 27, 2018 Through July 20, 2018, Because of Possible Listeria Monocytogenes Health Risk

G & C Raw, LLC is Expanding Recall to Include All Product Lots Manufactured from February 27, 2018 Through July 20, 2018, Because of Possible Listeria Monocytogenes Health Risk

G & C Raw, of Versailles, OH is recalling all products lots manufactured from February 27, 2018 through July 20, 2018, as a precaution because they have the potential to be contaminated with Listeria monocytogenes

FDA - U.S. Food and Drug Administration

24-10-2018

U-Pol Inc. recalls Automotive Repair and Refinish Products

U-Pol Inc. recalls Automotive Repair and Refinish Products

Health Canada has established that these products do not meet the mandatory warning labelling requirements for consumer use, as required under Canadian law. They are correctly labelled for workplace professional users, but the products lack the symbols and warnings required for consumer chemicals.

Health Canada

24-10-2018

Cub Cadet LLC recalls Cub Cadet RZT SX EFI Zero-Turn Riding Mower

Cub Cadet LLC recalls Cub Cadet RZT SX EFI Zero-Turn Riding Mower

The fill neck on the top of the fuel tank assembly of the affected mowers can experience stress cracking. This condition can cause fuel to leak from the fill neck during refilling or for the fill neck to shear off from the top of the fuel tank, posing a fire hazard.

Health Canada

24-10-2018

Vita Health Products Recall (2018-10-24)

Vita Health Products Recall (2018-10-24)

Health Canada

23-10-2018

New Seasons Market Issues Allergy Alert on Undeclared Soy in Hot & Sour Broth

New Seasons Market Issues Allergy Alert on Undeclared Soy in Hot & Sour Broth

New Seasons Market is recalling 193 jars of New Seasons Market Hot & Sour Broth because it contains undeclared soy. People who have an allergy or severe sensitivity to soy run the risk of serious or life-threatening allergic reaction if they consume these products.

FDA - U.S. Food and Drug Administration

23-10-2018

Shimano North America recalls Lazer Bicycle Helmets

Shimano North America recalls Lazer Bicycle Helmets

The recalled helmets do not meet the CPSC standard for the "Dynamic Roll Off" test. The helmet may come off on impact posing a head injury to the user.

Health Canada

23-10-2018

Zeagle recalls Sport Buoyancy Control Device Inflators

Zeagle recalls Sport Buoyancy Control Device Inflators

There exists a possibility that buttons on the Zeagle Sport BCD inflators may break or fracture leading to a rapid loss of air or auto inflation of the BCD, posing a potential drowning hazard.

Health Canada

22-10-2018

Promise Pharmacy Issues Voluntary Nationwide Recall of Prednisolone and Gatifloxacin Ophthalmic Solution 1%/0.5% Sterile Due to Small Particulate Floating in the Solution

Promise Pharmacy Issues Voluntary Nationwide Recall of Prednisolone and Gatifloxacin Ophthalmic Solution 1%/0.5% Sterile Due to Small Particulate Floating in the Solution

Promise Pharmacy is voluntarily recalling one lot of Prednisolone and Gatifloxacin Ophthalmic Solution 1%/0.5% sterile, 3ml vials, to the patient consumer level. The product has been found to have unidentified small particulate floating in the solution.

FDA - U.S. Food and Drug Administration

19-10-2018

Working Cow Homemade, Inc. Expands Recall of Ice Cream Products Because of Possible Health Risk

Working Cow Homemade, Inc. Expands Recall of Ice Cream Products Because of Possible Health Risk

Working Cow Homemade, Inc. of St. Petersburg, FL is expanding its voluntary recall to include all ice cream manufactured from August 29, 2017 – October 11, 2018, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nause...

FDA - U.S. Food and Drug Administration

2-11-2018

.@US_FDA  issues a class I recall: Roche Diagnostics recalls CoaguChek  XS PT Test  Strips due to inaccurate INR test results. Find out more:  https://go.usa.gov/xPVER  #FDA #MedicalDevicepic.twitter.com/EYmVZHrUZc

.@US_FDA issues a class I recall: Roche Diagnostics recalls CoaguChek XS PT Test Strips due to inaccurate INR test results. Find out more: https://go.usa.gov/xPVER  #FDA #MedicalDevicepic.twitter.com/EYmVZHrUZc

. @US_FDA issues a class I recall: Roche Diagnostics recalls CoaguChek XS PT Test Strips due to inaccurate INR test results. Find out more: https://go.usa.gov/xPVER  #FDA #MedicalDevice pic.twitter.com/EYmVZHrUZc

FDA - U.S. Food and Drug Administration