Nobilis Salmonella ET

Hauptinformation

  • Handelsname:
  • Nobilis Salmonella ET Injektionssuspension
  • Darreichungsform:
  • Injektionssuspension
  • Verwenden für:
  • Tiere
  • Art der Medizin:
  • allopathic Droge

Dokumenten

  • Information für medizinisches Fachpersonal:
  • Das Informationsblatt für dieses Produkt ist derzeit nicht verfügbar, können Sie eine Anfrage an unseren Kundendienst zu senden und wir werden Sie benachrichtigen, sobald wir in der Lage, um es zu erhalten.


    Fordern Sie die Packungsbeilage für medizinisches Fachpersonal.

Lokalisierung

  • Erhältlich in:
  • Nobilis Salmonella ET Injektionssuspension
    Belgien
  • Sprache:
  • Deutsch

Weitere Informationen

Status

  • Quelle:
  • AFMPS - Agence Fédérale des Médicaments et des Produits de Santé - Belgium
  • Zulassungsnummer:
  • BE-V266305
  • Letzte Änderung:
  • 17-04-2018

Packungsbeilage

B. PACKUNGSBEILAGE

Bijsluiter – DE Versie

Nobilis Salmonella ET

GEBRAUCHSINFORMATION FÜR

Nobilis Salmonella ET, injektionssuspension

1.

NAME UND ANSCHRIFT DES ZULASSUNGSINHABERS UND, WENN

UNTERSCHIEDLICH, DES HERSTELLERS, DER FÜR DIE CHARGENFREIGABE

VERANTWORTLICH IST

MSD Animal Health GmbH – Lynx Binnenhof 5 – 1200 Brüssel

Für die Chargenfreigabe verantwortlicher Hersteller: Intervet International B.V. - P.O. Box 31 - 5830

AA Boxmeer - die Niederlande

2.

BEZEICHNUNG DES TIERARZNEIMITTELS

Nobilis Salmonella ET, injektionssuspension

3.

WIRKSTOFFE UND SONSTIGE BESTANDTEILE

Pro Dosis (0,5 ml)

Wirkstoffe

Salmonella enteritidis PT4, Stamm 109 (Formalin inaktivierte Zellen)

1 x 10

Zellen,

induziert ≥ 1 RP*

Salmonella typhimurium DT104 (Formalin inaktivierte Zellen)

1 x 10

Zellen,

induziert ≥ 1 RP*

Hilfsstoffe:

Konservierungsmittel: Thiomersal

0,065 mg

* RP = relative potency = durchschnittliche Antikörperantwort im Kaninchen-Potencytest, größer als oder gleich zu einem

Referenzcharge deren Wirksamkeit bei Hühnern nachgewiesen wurde

4.

ANWENDUNGSGEBIETE

Zur aktiven Immunisierung von Hühnern, um die fäkale Ausscheidung von Salmonella enteritidis zu

verringern und die fäkale Ausscheidung von Salmonella typhimurium zeitlich zu verringern.

Aktive Immunität:

Beginn der Immunität: 4 Wochen nach der zweiten Impfung.

Immunitätsdauer: unbekannt

Zur passiven Immunisierung der Nachkommen um die fäkale Ausscheidung von Salmonella

enteritidis und S. typhimurium zu verringeren, angezeigt bis 7 Tagen nach der Infektion.

Passive Immunität:

Beginn der Immunität: 1 Tag nach dem Schlupf

Immunitätsdauer: bis 14 Tage nach dem Schlupf

Die passive Immunität wird 4 Wochen nach der zweiten Impfung bis zu einem Alter von mindestens

59 Wochen von den Elterntieren übertragen.

Zusätzliche Indikation: In Ausnahmefällen können Eintagsküken geimpft werden zur Schutz wenn sie

in einem jungen Alter während der Aufzucht in eine Umbegung kommen wo sie wahrscheinlich

infiziert werden sollen (epidemiologisch angezeigt auf Grund eines kürzlichen Ausbruches einer

Salmonellose oder eines hohen Infektionsdruckes an dieser Stelle).

Bijsluiter – DE Versie

Nobilis Salmonella ET

5.

GEGENANZEIGEN

Nicht bei Tieren in der Legephase anwenden.

6.

NEBENWIRKUNGEN

Der Impfstoff enthält ein Adjuvans und die Impfung kann eine vorübergehende Schwellung an der

Einstichstelle verursachen.

Bei Verabreichung einer Dosierung von 0,5 ml Nobilis Salmonella ET bei Hühnern ab einem Alter von

4 Wochen und älter, können ausnahmsweise unmittelbar nach der Impfung kleine tastbare Schwellung

(mit eine Maximalgrösse von 1cm

) auftreten an der Injektionsstelle; diese Schwellung halten

meistens nur 1 bis 2 Tagen an.

Die histopathologische Untersuchung der Einstichstelle 2 und 3 Wochen nach Verabreichung einer

Einzeldosis zeigte, dass die Impfung mit einer intramuskulären Entzündungsreaktion verbunden ist,

die eine Infiltration von Makrophagen und Plasmazellen zur Folge hat.

Nach der Impfung können auch vorübergehende Trägheit, Lethargie und Lahmheit auftreten, die bis zu

2 Tagen andauern.

Bei Eintagsküken (0,1 ml/Dosis) sind die Reaktionen ausgeprägter. In diesem Fall sollte berücksichtigt

werden, dass hier die Schwellungen an der Einstichstelle im Allgemeinen auffälliger sind als nach

Impfung von 0,5 ml bei Tieren ab einem Alter von 4 Wochen; gelegentlich kann der gesamte

Oberschenkel geschwollen sein.

Diese Reaktionen sind vorübergehend und in der Mehrzahl der Fälle nach 7 Tagen abgeklungen.

Ausnahmseweise kann eine Schwellung auch noch 15 Tage nach Impfung nachweisbar sein.

Darüber hinaus können nach der Impfung Anzeichen von Trägheit, Lethargie und Lahmheit sowie eine

Verringerung der Gewichtszunahme auftreten.

Falls Sie Nebenwirkungen insbesondere solche, die nicht in der Packungsbeilage

aufgeführt sind, bei Ihrem Tier feststellen, teilen Sie diese Ihrem Tierarzt mit.

7.

ZIELTIERARTEN

Hühner: Zuchttiere und Legehennen.

8.

DOSIERUNG FÜR JEDE TIERART, ART UND DAUER DER ANWENDUNG

Verabreichungsart

Standardimpfung: Intramuskuläre Injektion von 0,5 ml/Dosis.

Zur aktiven Immunisierung von Elterntieren und Legehennen:

zwei Impfungen im Abstand von 4 Wochen

Das empfohlene Impfalter beträgt 12 und 16 Wochen.

Notimpfung (wenn epidemiologisch angezeigt in einer risikoreichen Umgebung):

Intramuskuläre Injektion einer Dosis von 0,1 ml bei Eintagsküken.

Nach einem Intervall von 4 Wochen sollte eine Wiederholungsimpfung mit einer Dosis von 0,5 ml

verabreicht werden.

Zur passiven Immunisierung der Nachkommen von Elterntieren:

Zwei Impfungen im Abstand von 4 Wochen.

Das empfohlene Alter für die erste Impfung beträgt 6 - 12 Wochen, für die zweite Impfung 13 - 16

Wochen.

Bijsluiter – DE Versie

Nobilis Salmonella ET

Für den Fall, dass eine aktive und passive Immunität bei den Elterntieren bzw. deren Nachkommen

erzielt werden soll, sollte das Impfschema für die aktive Immunisierung befolgt werden.

9.

HINWEISE FÜR DIE RICHTIGE ANWENDUNG

Hygienemaßnahmen und gutes Management gehören ebenfalls zu einer Kontrollprogramm zur

Verringerung der Inzidenz von Salmonella-Infektionen.

10.

WARTEZEIT

Essbare Gewebe: Null Tage.

Nicht bei Tieren in der Legephase anwenden.

11.

BESONDERE LAGERUNGSHINWEISE

Arzneimittel unzugänglich für Kinder aufbewahren.

Vor Licht schützen.

Im Kühlschrank lagern (2

C – 8

Sie dürfen das Tierarzneimittel nach dem auf dem Karton angegebenen

Dauer der Haltbarkeit

Haltbarkeit des Tierarzneimittels im unversehrten Behältnis: 3 Jahre.

Haltbarkeit: nach Anbruch unverzüglich aufbrauchen.

12.

BESONDERE WARNHINWEISE

Besondere Vorsichtsmaßnahmen für die Anwendung bei Tieren

Es wurden keine Studien zum Einfluss maternaler Antikörper auf die Impfantwort durchgeführt. Daher

sollten Eintagsküken, wenn es epidemiologisch notwendig indiziert ist, nur dann mit Nobilis

Salmonella ET geimpft werden, wenn sie von nicht-geimpften und nicht-infizierten Elterntierherden

abstammen.

Die Impfung verursacht bei Hühnern eine serologische Antwort, die ein Überwachungsprogramm, das

nur auf serologischem Screening ohne bakteriologischem Nachweis basiert, beeinträchtigen kann. Der

Impfstoff sollte daher nicht eingesetzt werden, wenn die Erfassung des Infektionsstatus mit

Salmonella enteritidis und/oder Salmonella typhimurium ausschließlich auf einem serologischen

Screening beruht.

Die Impfung kann außerdem zu Kreuzreaktionen im Objektträger-Agglutinationstest mit S.

pullorum/gallinarum führen. Differentialdiagnostisch sollten in diesen Fällen spezifische serologische

und bakteriologische Methoden angewendet werden.

Anwendung während der Legeperiode

Nicht bei Tieren in der Legephase anwenden.

Wechselwirkungen mit anderen Arzneimitteln und andere Wechselwirkungen

Es liegen keine Informationen zur Unschädlichkeit und Wirksamkeit des Impfstoffesbei gleichzeitiger

Anwendung eines anderen veterinärmedizinischen Produktes vor. Ob der Impfstoff vor oder nach

Verabreichung eines anderen veterinärmedizinischen Produktes verwendet werden sollte, muss daher

fallweise entschieden werden.

Besondere Vorsichtsmaßnahmen für den Anwender

Bei versehentlicher Selbstinjektion ist unverzüglich ein Arzt zu Rate zu ziehen und das Etikett oder die

Packungsbeilage zeigen.

Bijsluiter – DE Versie

Nobilis Salmonella ET

13.

BESONDERE VORSICHTSMASSNAHMEN FÜR DIE ENTSORGUNG VON NICHT

VERWENDETEM ARZNEIMITTEL ODER VON ABFALLMATERIALIEN, SOFERN

ERFORDERLICH

Fragen Sie Ihren Tierarzt, wie nicht mehr benötigte Arzneimittel zu entsorgen sind. Diese Maßnahmen

dienen dem Umweltschutz.

14.

GENEHMIGUNGSDATUM DER PACKUNGSBEILAGE

August 2014

15.

WEITERE ANGABEN

Weise der Aushändigung: verschreibungspflichtig.

Zulassungsnummer: BE-V266305.

16-8-2018

Zakah Life Recalls Kratom Because Of Possible Health Risk

Zakah Life Recalls Kratom Because Of Possible Health Risk

Zakah Life, LLC of Ankeny, Iowa, is recalling the following Kratom products (Super Green Maeng Da Premium Kratom powder, Powerful Red Vein Bali Premium Kratom powder, Super Green Maeng Da Premium Kratom capsules, and Powerful Red Vein Bali Premium Kratom capsules) with expiration dates prior to 01/01/2023 because they have the potential of being contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weak...

FDA - U.S. Food and Drug Administration

14-8-2018

World Organix, LLC Issues Voluntary Nationwide Recall of Blissful Remedies Red Maeng Da 100% Mitragyna Speciosa, Blissful Remedies Red Maeng Da Liquid Kratom Mitragyna Speciosa, Blissful Remedies 4 Hour Chill Slow Motion Blend, Due to High Microbial Loads

World Organix, LLC Issues Voluntary Nationwide Recall of Blissful Remedies Red Maeng Da 100% Mitragyna Speciosa, Blissful Remedies Red Maeng Da Liquid Kratom Mitragyna Speciosa, Blissful Remedies 4 Hour Chill Slow Motion Blend, Due to High Microbial Loads

World Organix LLC, is voluntarily recalling lot: 112710 of Blissful Remedies Red Maeng Da 100% Mitragyna Speciosa capsules, Blissful Remedies Red Maeng Da Liquid Kratom Mitragyna Speciosa, Blissful Remedies 4 Hour Chill Slow Motion Blend to the consumer level. These products have been tested by the U.S. Food and Drug Administration (“FDA”) and found to be contaminated with High Microbial Loads. Additionally, this serves as a update to a previous press release posted on June 30th 2018, concerning Blissful...

FDA - U.S. Food and Drug Administration

25-7-2018

AMPI Recalls Limited Amount of Dry Whey Powder Because of Possible Health Risk

AMPI Recalls Limited Amount of Dry Whey Powder Because of Possible Health Risk

Associated Milk Producers Inc. (AMPI) of New Ulm, Minn., is recalling dry whey powder packaged in 50-pound and 25-kg bags that were produced at the cooperative’s Blair, Wis., dry whey plant from May 1-5, 2018; May 24-29, 2018; June 2-5, 2018; and June 7-14, 2018 due to the potential to be contaminated with Salmonella. This is a precautionary recall. All products shipped to the marketplace tested negative for Salmonella.

FDA - U.S. Food and Drug Administration

24-7-2018

Pepperidge Farm® Announces Voluntary Recall of Four Varieties of Goldfish® Crackers

Pepperidge Farm® Announces Voluntary Recall of Four Varieties of Goldfish® Crackers

Pepperidge Farm has been notified by one of its ingredient suppliers that whey powder in a seasoning that is applied to four varieties of crackers has been the subject of a recall by the whey powder manufacturer due to the potential presence of Salmonella. Pepperidge Farm initiated an investigation and, out of an abundance of caution, is voluntarily recalling four varieties of Goldfish crackers. The products were distributed throughout the United States. No illnesses have been reported. ...

FDA - U.S. Food and Drug Administration

24-7-2018

Statement from FDA Commissioner Scott Gottlieb, M.D. on voluntary recalls of Ritz, Goldfish and other products issued out of an abundance of caution

Statement from FDA Commissioner Scott Gottlieb, M.D. on voluntary recalls of Ritz, Goldfish and other products issued out of an abundance of caution

The U.S. Food and Drug Administration is working with Mondelēz International, Inc., Pepperidge Farm Inc. and Flowers Foods, Inc. to initiate voluntarily recalls of certain products due to a potential risk that one of the ingredients may have been contaminated with Salmonella.

FDA - U.S. Food and Drug Administration

23-7-2018

Flowers Foods Issues Voluntary Recall on Mrs. Freshley’s and Other Brands of Swiss Rolls and Captain John Derst’s Old Fashioned Bread

Flowers Foods Issues Voluntary Recall on Mrs. Freshley’s and Other Brands of Swiss Rolls and Captain John Derst’s Old Fashioned Bread

As a precautionary measure, Flowers Foods, Inc. (NYSE: FLO) is voluntarily recalling Swiss Rolls sold under the brand names Mrs. Freshley’s, Food Lion, H-E-B, Baker’s Treat, Market Square, and Great Value, distributed nationwide, and Captain John Derst’s Old Fashioned Bread distributed in Alabama, Florida, Georgia, North Carolina, and South Carolina, due to the potential presence of Salmonella in an ingredient, whey powder. The ingredient recall was initiated by a third-party whey powder manufacturer and...

FDA - U.S. Food and Drug Administration

23-7-2018

Mondelēz Global LLC Conducts Voluntary Recall of Certain Ritz Cracker Sandwiches and Ritz Bits Product in the U.S., including Puerto Rico & U.S. Virgin Islands Due to Possible Health Risk

Mondelēz Global LLC Conducts Voluntary Recall of Certain Ritz Cracker Sandwiches and Ritz Bits Product in the U.S., including Puerto Rico & U.S. Virgin Islands Due to Possible Health Risk

Mondelēz Global LLC announced today a voluntary recall in the United States, including Puerto Rico & the U.S. Virgin Islands, of certain Ritz Cracker Sandwiches and Ritz Bits product. These products contain whey powder as an ingredient, which the whey powder supplier has recalled due to the potential presence of Salmonella.

FDA - U.S. Food and Drug Administration

18-7-2018

FDA Investigating Multistate Outbreak of Salmonella Sandiego Infections Linked to Hy-Vee Spring Pasta Salad

FDA Investigating Multistate Outbreak of Salmonella Sandiego Infections Linked to Hy-Vee Spring Pasta Salad

The U.S. Food and Drug Administration, along with the Centers for Disease Control and Prevention (CDC) and state and local partners, is investigating a multi-state outbreak of Salmonella Sandiego illnesses linked to Spring Pasta Salad sold at Hy-Vee locations in Iowa, Illinois, Kansas, Minnesota, Missouri, Nebraska, South Dakota, and Wisconsin.

FDA - U.S. Food and Drug Administration

18-7-2018

Hy-Vee Voluntarily Recalls Spring Pasta Salad Due to Reported Illnesses

Hy-Vee Voluntarily Recalls Spring Pasta Salad Due to Reported Illnesses

WEST DES MOINES, Iowa (July 17, 2018) — Hy-Vee, Inc., based in West Des Moines, Iowa, is voluntarily recalling its Hy-Vee Spring Pasta Salad due to the potential that it may be contaminated with Salmonella. The potential for contamination was brought to Hy-Vee’s attention last night when approximately 20 illnesses in Minnesota, South Dakota, Nebraska and Iowa were potentially linked back to customers consuming the salad. The voluntary recall includes Hy-Vee Spring Pasta Salads in both 1 pound (16 oz.) an...

FDA - U.S. Food and Drug Administration

2-7-2018

Blissful Remedies Issues Voluntary Nationwide Recall of Certain Kratom Powder Capsule

Blissful Remedies Issues Voluntary Nationwide Recall of Certain Kratom Powder Capsule

Blissful Remedies., is voluntarily recalling only Lot No.: 112710 with expiration 03/2019 found embedded on the top of package of kratom ( mitragyn a speciosa) powder products, it manufactured, processed, packed, and/or held, between “March 1, 2018” to “April 30, 2018” to the consumer level. The products have been found by the U.S. Food and Drug Administration (“FDA”) via sample testing to have salmonella contamination. Blissful Remedies has not received reports of adverse events related to this recall. ...

FDA - U.S. Food and Drug Administration

22-6-2018

Kratom (mitragyna speciosa) Powder Products by Gaia Ethnobotanical: Recall - Due to Potential Salmonella Contamination

Kratom (mitragyna speciosa) Powder Products by Gaia Ethnobotanical: Recall - Due to Potential Salmonella Contamination

The products have been found by the FDA via sample testing and finding to have salmonella contamination. In lieu of such FDA findings the company has implemented standard operating procedures and sterilization processes in accordance to FDA guidelines

FDA - U.S. Food and Drug Administration

21-6-2018

Gaia Ethnobotanical, LLC., Voluntarily Recalls Kratom Products Due to Potential Salmonella Contamination

Gaia Ethnobotanical, LLC., Voluntarily Recalls Kratom Products Due to Potential Salmonella Contamination

Gaia Ethnobotanical, LLC., is voluntarily recalling all kratom (mitragyna speciosa) powder products, with Lot No.: 0102031800 it manufactured, processed, packed, and/or held, between March 18, 2018 to March 30, 2018 to the consumer level. The products have been found by the U.S. Food and Drug Administration (“FDA”) via sample testing and finding to have salmonella contamination. In lieu of such FDA findings the company has implemented standard operating procedures and sterilization processes in accordanc...

FDA - U.S. Food and Drug Administration

21-6-2018

Now Health Group Inc. Recalls Select Now Real Food® Zesty Sprouting Mix Because of Possible Health Risk

Now Health Group Inc. Recalls Select Now Real Food® Zesty Sprouting Mix Because of Possible Health Risk

NOW Health Group, Inc. (NOW), of Bloomingdale, Illinois, is recalling its NOW Real Food® Zesty Sprouting Mix – Product Code 7271, Lot #3031259 and Lot #3038165 – because its primary ingredient, Crimson Clover Seeds, has the potential to be contaminated with Salmonella, an organism which 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 b...

FDA - U.S. Food and Drug Administration

15-6-2018

FDA Investigating Multistate Outbreak of Salmonella Mbandaka Infections Likely Linked to Kellogg’s Honey Smacks Cereal

FDA Investigating Multistate Outbreak of Salmonella Mbandaka Infections Likely Linked to Kellogg’s Honey Smacks Cereal

The U.S. Food and Drug Administration, along with the Centers for Disease Control and Prevention (CDC) and state and local partners, are investigating a multistate outbreak of Salmonella Mbandaka illnesses that may be linked to Kellogg’s Honey Smacks cereal.

FDA - U.S. Food and Drug Administration

15-6-2018

Kellogg Company Voluntarily Recalls Honey Smacks Cereal Due to Possible Health Risk

Kellogg Company Voluntarily Recalls Honey Smacks Cereal Due to Possible Health Risk

Kellogg Company today announced it is voluntarily recalling 15.3 oz. and 23 oz. packages of Kellogg’s® Honey Smacks® cereal (with code dates listed below) because these products have the potential presence of Salmonella. No other Kellogg products are impacted by this recall.

FDA - U.S. Food and Drug Administration

9-6-2018

Caito Foods, LLC Voluntarily Recalls Fresh Cut Melon Products Because of Possible Health Risk

Caito Foods, LLC Voluntarily Recalls Fresh Cut Melon Products Because of Possible Health Risk

Caito Foods is voluntarily recalling fresh cut watermelon, honeydew melon, cantaloupe and fresh-cut mixed fruit containing one of these melons, produced at the Caito Foods facility in Indianapolis, because these products have the potential to be contaminated with Salmonella.

FDA - U.S. Food and Drug Administration

9-6-2018

FDA Investigating Multistate Outbreak of Salmonella Adelaide Infections Linked to Pre-Cut Melons

FDA Investigating Multistate Outbreak of Salmonella Adelaide Infections Linked to Pre-Cut Melons

The U.S. Food and Drug Administration, along with the Centers for Disease Control and Prevention (CDC) and state and local partners, are investigating a multistate outbreak of Salmonella Adelaide illnesses that may be linked to cut melons.

FDA - U.S. Food and Drug Administration

6-6-2018

Nobilis IB 4-91 ad us. vet.

Nobilis IB 4-91 ad us. vet.

● Änderung Text alle Rubriken

Institut für Veterinärpharmakologie und toxikologie

6-6-2018

Nobilis IB Ma5 ad us. vet.

Nobilis IB Ma5 ad us. vet.

● Änderung Text alle Rubriken

Institut für Veterinärpharmakologie und toxikologie

29-5-2018

Pious Lion Voluntary Recall Due to Possible Health Risk

Pious Lion Voluntary Recall Due to Possible Health Risk

Pious Lion located in Asheville, NC is voluntarily recalling two of their Kratom products: Pious Lion Pure Premium Potent Limited Release Pink Bali, 1 oz and Pious Lion Pure Premium Potent White Maeng DA, Bright Uplifting Energy, 4 oz due to the presence of Salmonella . Salmonella is an organism which 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, diarrhe...

FDA - U.S. Food and Drug Administration

23-5-2018

Golden International Corporation  Issues Public Safety Warning For Stolen Tilapia Because  of Possible Health Risk

Golden International Corporation Issues Public Safety Warning For Stolen Tilapia Because of Possible Health Risk

Golden International Corporation of Renton, WA is issuing a public safety notice for 405 cartons of stolen frozen tilapia, because it has the potential to be contaminated with Salmonella, an organism which 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. In rare circumstances, infection wi...

FDA - U.S. Food and Drug Administration

21-5-2018

Ziyad Brothers Importing Recalls Tahini Because of Possible Health Risk

Ziyad Brothers Importing Recalls Tahini Because of Possible Health Risk

Ziyad Brothers Importing is voluntarily recalling certain lot codes of Ziyad Brand Tahini because it has the potential to be contaminated with Salmonella, an organism which 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, nausea, vomiting, and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into ...

FDA - U.S. Food and Drug Administration

4-5-2018

Badger Botanicals Recalls Red Suma, Green Suma, Green Hulu 2, And Red Hulu 2 Kratom Supplements Because Of Possible Salmonella Health Risk

Badger Botanicals Recalls Red Suma, Green Suma, Green Hulu 2, And Red Hulu 2 Kratom Supplements Because Of Possible Salmonella Health Risk

Badger Botanicals, LLC of Springville, Utah is recalling Green Suma, Red Suma, Green Hulu 2, and Red Hulu 2 kratom dietary supplements sold directly to consumers via the company website from January 1st, 2018 to April l 12th, 2018 in pouches of 250g, because it has the potential to be contaminated with Salmonella.

FDA - U.S. Food and Drug Administration

4-5-2018

Maya Distribution, LLC Recalls Dragon Label Kratom Because Of Possible Salmonella Contamination

Maya Distribution, LLC Recalls Dragon Label Kratom Because Of Possible Salmonella Contamination

Maya Distribution, LLC of South Salt Lake City, Utah is voluntarily recalling Dragon Kratom labeled bottles and sealed packages of encapsulated and raw powder product because it has the potential to be contaminated with Salmonella, 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

24-4-2018

One lot of Traditional Medicinals "Throat Coat Lemon Echinacea" herbal tea recalled because of potential contamination with Salmonella

One lot of Traditional Medicinals "Throat Coat Lemon Echinacea" herbal tea recalled because of potential contamination with Salmonella

Health Canada is advising Canadians that one lot of “Throat Coat Lemon Echinacea” herbal tea is being voluntarily recalled by Traditional Medicinals after a company supplier found Salmonella contamination in a tea ingredient (lemon myrtle leaf). An infection caused by Salmonella bacteria may pose serious health risks, particularly for young children, pregnant women, the elderly and people with weak immune systems.

Health Canada

20-4-2018

Dietary Supplements by Nutrizone: Recall - Potential for Salmonella Contamination

Dietary Supplements by Nutrizone: Recall - Potential for Salmonella Contamination

Expanded recall of various kratom dietary supplements to additional lot numbers due to possible Salmonella Health Risk.

FDA - U.S. Food and Drug Administration

19-4-2018

Certain Kratom-Containing Powder Products by Viable Solutions: Recall -Possible Salmonella Contamination

Certain Kratom-Containing Powder Products by Viable Solutions: Recall -Possible Salmonella Contamination

Viable Solutions of Nampa, ID has initiated a recall of certain Kratom-containing powder products, because it has the potential to be contaminated with Salmonella, an organism which 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. In rare circumstances, infection with Salmonella can result...

FDA - U.S. Food and Drug Administration

19-4-2018

NxtGen Botanicals Maeng Da Kratom by NGB Corp.: Recall - Possible Salmonella Contamination

NxtGen Botanicals Maeng Da Kratom by NGB Corp.: Recall - Possible Salmonella Contamination

NGB Corp. of West Jordan, Utah is voluntarily recalling NxtGen Botanicals Maeng Da Kratom labeled bottles of encapsulated product because it has the potential to be contaminated with Salmonella, an organism which 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. In rare circumstances, infec...

FDA - U.S. Food and Drug Administration

6-4-2018

"Organic Traditions Shatavari Powder" sold at Choices Markets Yaletown in Vancouver, B.C., contaminated with Salmonella

"Organic Traditions Shatavari Powder" sold at Choices Markets Yaletown in Vancouver, B.C., contaminated with Salmonella

Health Canada is advising Canadians that one lot of “Organic Traditions Shatavari Powder” is being voluntarily recalled by Advantage Health Matters Inc. Company testing found Salmonella bacteria contamination, which may pose serious health risks. According to Advantage Health Matters Inc., 13 units from the affected lot were distributed. Of the 13 units, only 2 packages, sold at Choices Markets Yaletown (1202 Richards Street) in Vancouver, B.C., have not been recovered.

Health Canada

Es gibt keine Neuigkeiten betreffend dieses Produktes.