ESPITONE

Main information

  • Trade name:
  • ESPITONE 200ML SYR
  • Pharmaceutical form:
  • SYR
  • Composition:
  • 200ML
  • Medicine domain:
  • Humans
  • Medicine type:
  • Allopathic drug

Documents

Localization

  • Available in:
  • ESPITONE 200ML SYR
    India
  • Language:
  • English

Other information

Status

  • Source:
  • Central Drugs Standard Control Organization
  • Last update:
  • 09-08-2016

21-4-2018

OC Raw Dog, LLC RECALLS Freeze Dried Sardines BECAUSE PRODUCT EXCEEDS FDA SIZE RESTRICTIONS

OC Raw Dog, LLC RECALLS Freeze Dried Sardines BECAUSE PRODUCT EXCEEDS FDA SIZE RESTRICTIONS

OC Raw Dog, LLC of Rancho Santa Margarita, CA, is recalling the Freeze Dried Sardines because the fish have exceeded the FDA compliance guideline for fish larger than 5 inches.

FDA - U.S. Food and Drug Administration

19-4-2018

NGB Corp. Recalls NxtGen Botanicals Maeng Da Kratom Because of Possible <em>Salmonella</em> Contamination

NGB Corp. Recalls NxtGen Botanicals Maeng Da Kratom Because of Possible <em>Salmonella</em> 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.

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

18-4-2018

TruPet LLC Recalls Boost Me Mighty Meaty Beef Topper Meal Enhancer Because of Possible <em>Salmonella</em> Contamination

TruPet LLC Recalls Boost Me Mighty Meaty Beef Topper Meal Enhancer Because of Possible <em>Salmonella</em> Contamination

TruPet, LLC of Milford, OH, is voluntarily recalling a limited amount of Boost Me Mighty Meaty Beef Topper Meal Enhancer because the products have the potential to be contaminated with Salmonella. The recall is limited to 400 cases of the product, as identified below.

FDA - U.S. Food and Drug Administration

17-4-2018

Medline Canada, Corp. recalls Remedy Essentials Foaming Cleanser

Medline Canada, Corp. recalls Remedy Essentials Foaming Cleanser

The affected product is contaminated with the bacteria Burkolderia cepacia. Burkolderia cepacia can pose a risk of infections to consumers, especially those with weakened immune systems.

Health Canada

16-4-2018

Acupuncture needles with false CE marking

Acupuncture needles with false CE marking

Sterile acupuncture needles with false CE marking are sold online. We ask you to pay attention to these products because there is no documentation to support the product's sterility or the materials used to fabricate the device.

Danish Medicines Agency

14-4-2018

Urgent: Voluntary Product Recall of Vuse Vibe Power Units

Urgent: Voluntary Product Recall of Vuse Vibe Power Units

R.J. Reynolds Vapor Company has voluntarily initiated a nationwide safety recall of all Vuse Vibe power units. The Company initiated the recall after receiving consumer complaints about malfunctioning batteries, which may cause the power unit to overheat and create a fire risk. The Company notified the U.S. Food and Drug Administration regarding the issue and will be working directly with the Agency on this voluntary recall.

FDA - U.S. Food and Drug Administration

14-4-2018

'Rhino 69 Extreme 50000' Recalled due to Presence of Active Ingredient 'Tadalafil'

'Rhino 69 Extreme 50000' Recalled due to Presence of Active Ingredient 'Tadalafil'

AMA Wholesale Inc. (Distributor/Re-seller), is voluntarily recalling Rhino 69 Extreme 50000 capsules to the consumer level. FDA analysis found the product to be tainted with undeclared tadalafil. Tadalafil is an active ingredient in a FDA-approved prescription drug that is used for erectile dysfunction.

FDA - U.S. Food and Drug Administration

13-4-2018

Guixens Food Group Issues Allergy Alert on Undeclared Sulfites in La Marinera Brand Dried Yellow Potatoes

Guixens Food Group Issues Allergy Alert on Undeclared Sulfites in La Marinera Brand Dried Yellow Potatoes

Guixens Food Group, Inc., of Miami, FL, is voluntarily recalling its ten-ounce packages of La Marinera Brand Dried Yellow Potatoes because it may contain undeclared sulfites. People who have an allergy or severe sensitivity to sulfites run the risk of serious or life-threatening allergic reaction if they consume this product.

FDA - U.S. Food and Drug Administration

12-4-2018

Cookwell & Company Issues Allergy Alert for Undeclared Soy, Wheat and Fish Allergen in Charred Tomato & Basil Sauce with a “Best By” Date of “10 Nov 18”

Cookwell & Company Issues Allergy Alert for Undeclared Soy, Wheat and Fish Allergen in Charred Tomato & Basil Sauce with a “Best By” Date of “10 Nov 18”

Cookwell & Company Is voluntarily recalling potentially up to 6,522 units of its Four J Charred Tomato & Basil Sauce because it may contain undeclared soy, wheat and fish. People who have an allergy or severe sensitivity to these allergens may run the risk of a serious or life-threatening allergic reaction if they consume this product.

FDA - U.S. Food and Drug Administration

11-4-2018

Premier Pharmacy Labs Issues Voluntary Nationwide Recall of Specific Sterile Injectable Products Lots Due to a Potential Lack of Sterility Assurance

Premier Pharmacy Labs Issues Voluntary Nationwide Recall of Specific Sterile Injectable Products Lots Due to a Potential Lack of Sterility Assurance

Microbial contamination was detected during routine testing of subsequent unreleased product lots due to interaction between the product syringe and tamper evident container closure, which may result in the potential introduction of microorganisms into the products.

FDA - U.S. Food and Drug Administration

9-4-2018

Stewart’s Shops Issues Allergy Alert on Pint Chocolate Peanut Butter Cup Ice Cream

Stewart’s Shops Issues Allergy Alert on Pint Chocolate Peanut Butter Cup Ice Cream

Stewart’s Shops Corp. is recalling units of Stewart’s pint Chocolate Peanut Butter Cup ice cream because they may have been packaged incorrectly with a “Chocolate” lid. People who have an allergy to peanuts run the risk of serious or life-threatening allergic reaction if they consume this product.

FDA - U.S. Food and Drug Administration

7-4-2018

Advocare Issues Allergy Alert in Select Bottles of Muscle Strength and Nighttime Recovery Product Because of Undeclared Milk Allergen on The Label

Advocare Issues Allergy Alert in Select Bottles of Muscle Strength and Nighttime Recovery Product Because of Undeclared Milk Allergen on The Label

AdvoCare International has commenced a voluntary recall of two lots of Muscle Strength and four lots of Nighttime Recovery dietary supplements because they may contain undeclared milk that can elicit an allergic reaction in individuals who are sensitive to milk and milk products.

FDA - U.S. Food and Drug Administration

5-4-2018

3M Canada recalls 3M ScotchTM Thermal Laminator

3M Canada recalls 3M ScotchTM Thermal Laminator

The plastic housing on the bottom of the product may become overheated, causing the housing to deform. The deformed plastic may pose a potential risk of burn if the product were to be touched on the bottom at the time of overheating.

Health Canada

2-4-2018

Pasta De Lassar Andromaco Skin Protectant 25 Percent Zinc Oxide by MarcasUSA: Recall - Potential Contamination

Pasta De Lassar Andromaco Skin Protectant 25 Percent Zinc Oxide by MarcasUSA: Recall - Potential Contamination

Use of the contaminated product could result in an increased risk of infection.

FDA - U.S. Food and Drug Administration

2-4-2018

New York raw milk cheese company ordered to stop sales for food safety violations

New York raw milk cheese company ordered to stop sales for food safety violations

FDA announces an enforcement action taken against Vulto Creamery of New York. The company cannot sell ready-to-eat raw cheese product until it complies with the consent decree. Vulto was linked to an outbreak last year.

FDA - U.S. Food and Drug Administration

30-3-2018

MarcasUSA, LLC Issues Voluntary Nationwide Recall of Pasta De Lassar Andromaco Skin Protectant 25% Zinc Oxide 60g Due to Potential Contamination

MarcasUSA, LLC Issues Voluntary Nationwide Recall of Pasta De Lassar Andromaco Skin Protectant 25% Zinc Oxide 60g Due to Potential Contamination

FOR IMMEDIATE RELEASE – March 29, 2018 – El Segundo, CA, MarcasUSA, LLC and Industria Farmacéutica Andromaco, S.A. de C.V. is voluntarily recalling four lots of Pasta De Lassar Andromaco Skin Protectant, 25% zinc oxide to the retail level. FDA analysis of this product confirmed that Pasta De Lassar Andromaco is contaminated with high levels of yeast, mold, and bacteria. The specific lot associated to the positive findings was never sold in the US. However, due to the amount and type of contamination t...

FDA - U.S. Food and Drug Administration

28-3-2018

CBER-Regulated Products: Shortages and Discontinuations

CBER-Regulated Products: Shortages and Discontinuations

A CBER-regulated product shortage occurs when a CBER-regulated product is not commercially available in sufficient quantity to meet the demand.

FDA - U.S. Food and Drug Administration

28-3-2018

Public Notification: Black Lion Pill contains hidden drug ingredient

Public Notification: Black Lion Pill contains hidden drug ingredient

The Food and Drug Administration is advising consumers not to purchase or use Black Lion Pill, a product promoted and sold for sexual enhancement on various websites, including www.rakuten.com, and possibly in some retail stores.

FDA - U.S. Food and Drug Administration

28-3-2018

Public Notification: Rhino 69 Extreme 50000 contains hidden drug ingredient

Public Notification: Rhino 69 Extreme 50000 contains hidden drug ingredient

The Food and Drug Administration is advising consumers not to purchase or use Rhino 69 Extreme 50000, a product promoted and sold for sexual enhancement on various websites, including www.bonanza.com, and possibly in some retail stores.

FDA - U.S. Food and Drug Administration

28-3-2018

Public Notification: Red Zone Xtreme 3000 contains hidden drug ingredient

Public Notification: Red Zone Xtreme 3000 contains hidden drug ingredient

The Food and Drug Administration is advising consumers not to purchase or use Red Zone Xtreme 3000, a product promoted and sold for sexual enhancement on various websites, including www.ebay.com, and possibly in some retail stores.

FDA - U.S. Food and Drug Administration

28-3-2018

DKMA Update March 2018

DKMA Update March 2018

In this issue of DKMA Update you can read about evidence; changes to Tramadol’s summary of product characteristics; inspections of the sale of OTC medicines outside pharmacies and much more

Danish Medicines Agency

28-3-2018

First Source Issues Allergy Alert on Undeclared Peanuts in Wegmans 9 Oz Yogurt Raisins

First Source Issues Allergy Alert on Undeclared Peanuts in Wegmans 9 Oz Yogurt Raisins

First Source of Tonawanda, NY, is voluntarily recalling 9 OZ packages of Wegmans Yogurt Raisins, because the product may contain undeclared peanuts. People who have an allergy or sensitivity to peanuts run the risk of serious or life- threatening allergic reaction if they consume this product.

FDA - U.S. Food and Drug Administration

27-3-2018

Allergy Alert Issued in Select Northern California Whole Foods Market Stores for Undeclared Egg in Some Cookies

Allergy Alert Issued in Select Northern California Whole Foods Market Stores for Undeclared Egg in Some Cookies

Nine Whole Foods Market stores in Northern California are voluntarily recalling some decorated (iced) cookies from the self-service cookie displays because the products contained egg allergen that was not listed on the product sign. People who have an allergy or severe sensitivity to eggs run the risk of serious or life-threatening allergic reaction if they consume these products.

FDA - U.S. Food and Drug Administration

26-3-2018

Blue Ridge Beef Voluntarily Recalls BRB Complete Raw Pet Food Lot#GA0131 Because of Possible Contamination

Blue Ridge Beef Voluntarily Recalls BRB Complete Raw Pet Food Lot#GA0131 Because of Possible Contamination

Blue Ridge Beef of Eatonton, GA, is voluntarily recalling lot#GA0131 of BRB Complete raw pet food because of the potential of contamination with Salmonella and Listeria monocytogenes. The cause of the recall: This recall was initiated after samples collected and tested by the FDA showed positive for Salmonella and Listeria monocytogenes. There has been no consumer or pet illnesses in association with this product. Blue Ridge Beef is voluntarily recalling this product lot as a commitment to consumer and p...

FDA - U.S. Food and Drug Administration

16-3-2018

Chris’s Cookies Recalls Chocolate Chip Cookies Due to Undeclared Peanuts

Chris’s Cookies Recalls Chocolate Chip Cookies Due to Undeclared Peanuts

Teterboro, NJ (March 15, 2018) - Chris’s Cookies has recalled one lot of its Trader Joe’s Chocolate Chip Cookie 12 Oz (340g) Bags (Barcode#: 0068 0752) after a report that Peanut Butter Chocolate Chip Cookies were discovered in a Chocolate Chip Cookie Bag, and therefore the product may contain undeclared peanuts. People who have an allergy to peanuts run the risk of serious or life-threatening allergic reaction if they eat this product.

FDA - U.S. Food and Drug Administration

16-3-2018

Alka-Seltzer Plus Products: Recall - Ingredients on Front Sticker May Not Match Product in Carton

Alka-Seltzer Plus Products: Recall - Ingredients on Front Sticker May Not Match Product in Carton

Consumers may ingest a product to which they may have an allergy or anaphylactic reaction, an ingredient which may be contraindicated for their condition or they intend to otherwise avoid, with potential for serious health consequences.

FDA - U.S. Food and Drug Administration

16-3-2018

Bayer Issues Voluntary Recall of Alka-Seltzer Plus® Products

Bayer Issues Voluntary Recall of Alka-Seltzer Plus® Products

Bayer is voluntarily recalling Alka-Seltzer Plus® packages that: • Were sold only in the U.S. at Walmart, CVS, Walgreens and Kroger (including Dillons Food Stores, Fred Meyer, Fry’s Food Stores, Ralphs, King Soopers and Smith’s Food and Drug) after February 9, 2018. • Can be identified by checking the Bayer logo located on the lower left corner of the front of the carton. If the logo has an orange or green background, the product is included in the recall (please see attached photos). The affected...

FDA - U.S. Food and Drug Administration

15-3-2018

Handi-Craft Company recalls various Dr. Brown's Lovey Pacifier & Teether Holders

Handi-Craft Company recalls various Dr. Brown's Lovey Pacifier & Teether Holders

Repeated use and wear of the product can cause the pacifier ribbons to fray and/or unravel, allowing the snaps to inadvertently detach from the ribbon and pose a potential choking hazard.

Health Canada

15-3-2018

Louis Garneau Sports Inc. recalls Course LG1261 Cycling Helmets

Louis Garneau Sports Inc. recalls Course LG1261 Cycling Helmets

The plastic shell on the helmet can weaken over time causing the product to fail head impact testing. In the event of an accident, the helmet could fail to prevent head injuries, posing a hazard to consumers.

Health Canada

14-3-2018

Sexual enhancement product "Leopard Miracle of Honey" may pose serious health risks

Sexual enhancement product "Leopard Miracle of Honey" may pose serious health risks

Health Canada is advising Canadians that two versions of the sexual enhancement product “Leopard Miracle of Honey” may pose serious health risks. Both versions are labelled as being approved by Health Canada, with NPN 80073650. Health Canada’s testing found that both versions of the product contain the undeclared prescription drug sildenafil. The product was not authorized to contain this prescription drug. Health Canada seized the products from two Ontario convenience stores located in Woodbridge, ON, a...

Health Canada

13-3-2018

Oregon Food Bank Issues Alert on Foreign Material in Chia Seeds

Oregon Food Bank Issues Alert on Foreign Material in Chia Seeds

Oregon Food Bank of Portland, Oregon has initiated a Class II recall of 22,201 pounds of chia seeds, which were donated to the food bank. The product may be contaminated with rodent droppings. While no known illnesses have been associated with this product, use or consumption may present a health hazard to consumers.

FDA - U.S. Food and Drug Administration

12-3-2018

Wegmans Food Markets Issues Allergen Alert on Undeclared Egg in Wegmans Thai Sweet Chili Sauce Cup 1.5 oz. Sold in the Sushi Department

Wegmans Food Markets Issues Allergen Alert on Undeclared Egg in Wegmans Thai Sweet Chili Sauce Cup 1.5 oz. Sold in the Sushi Department

Wegmans Food Markets, Inc. is recalling Wegmans Thai Sweet Chili Sauce Cup 1.5 oz. (UPC7-66630-98023) with a best-by of 7/4/18 or 7/5/18 because the product may contain undeclared egg. People who have an allergy or severe sensitivity to egg run the risk of serious or life-threatening allergic reaction if they consume this product.

FDA - U.S. Food and Drug Administration

12-3-2018

Consumer Alert: <em> Listeria </em> Contamination In Maiden’s Creamery Wild Meadow Raw Goat Milk Cheese

Consumer Alert: <em> Listeria </em> Contamination In Maiden’s Creamery Wild Meadow Raw Goat Milk Cheese

New York State Agriculture Commissioner Richard Ball today warned consumers not to consume The Maiden’s Creamery “Wild Meadow” Raw Goat Milk Cheese made by Mark Harvey, 1277 Copes Corner Road, South New Berlin, NY 13843 due to possible Listeria contamination. To date, no illnesses have been reported to the Department in connection with this product.

FDA - U.S. Food and Drug Administration

9-3-2018

Starwest Botanicals Inc. Product Recalls Organic Cardamom Pods Green (Whole) Due to Possible <em>Salmonella</em> Contamination

Starwest Botanicals Inc. Product Recalls Organic Cardamom Pods Green (Whole) Due to Possible <em>Salmonella</em> Contamination

Starwest Botanicals is voluntarily recalling Starwest Botanicals Organic Cardamom Pods Green (Whole), which is packaged in Mylar 1 pound bags and in bulk packs.

FDA - U.S. Food and Drug Administration

9-3-2018

Auto-Chem Inc. recalls FREE-SHINE product

Auto-Chem Inc. recalls FREE-SHINE product

Health Canada’s sampling and evaluation program has determined that the products identified do not meet the labelling requirements for chemical consumer products as set out in the Canada Consumer Product Safety Act (CCPSA).

Health Canada

8-3-2018

Redbarn Pet Products Expands Voluntary Recall of Dog Chews

Redbarn Pet Products Expands Voluntary Recall of Dog Chews

Redbarn Pet Products, LLC of Long Beach, CA is expanding their voluntarily recall initially issued on February 9th. The recall expanded to include all lots of product manufactured with raw material from a single supplier because it has the potential to be contaminated with Salmonella. The recall is limited to products distributed March 2017 through February 2018. This supplier’s raw material was used to produce the Redbarn, Chewy Louie, Dentley’s and Good Lovin’ brand products listed below with best-buy ...

FDA - U.S. Food and Drug Administration

8-3-2018

Ciolo Foods Issues Allergy Alert for Undeclared Tree Nuts in “Ciolo Nut-Free Basil

Ciolo Foods Issues Allergy Alert for Undeclared Tree Nuts in “Ciolo Nut-Free Basil

Ciolo Foods of Lafayette, CO has voluntarily recalled it’s 7-ounce containers of “Nut-Free Basil Pesto” because they contain undeclared tree nuts (Pine Nuts and Walnuts). People who have allergies or severe sensitivity to Pine Nuts and/or Walnuts run the risk of serious allergic reaction if they consume this product.

FDA - U.S. Food and Drug Administration

6-3-2018

Methylprednisolone Sodium Succinate for Injection 40mg, 125mg, and 1g by Sagent Pharmaceuticals: Recall - High Out of Specification Impurity Results

Methylprednisolone Sodium Succinate for Injection 40mg, 125mg, and 1g by Sagent Pharmaceuticals: Recall - High Out of Specification Impurity Results

An elevated impurity has the potential to decrease effectiveness of the product in patients. Posted: 03/06/2018

FDA - U.S. Food and Drug Administration

6-3-2018

Kodiak Cakes Issues Allergy Alert on Undeclared Milk in Kodiak Cakes Blueberry Chia Energy Waffles 10.72 oz. Product UPC code is 7 05599 01215 0.

Kodiak Cakes Issues Allergy Alert on Undeclared Milk in Kodiak Cakes Blueberry Chia Energy Waffles 10.72 oz. Product UPC code is 7 05599 01215 0.

Kodiak Cakes of Park City, UT is recalling all lots and codes of Kodiak Cakes Blueberry Chia Energy Waffles 10.72 oz that were on shelf prior to March 5, 2018 because they contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

FDA - U.S. Food and Drug Administration

1-3-2018

The Double Cola Company Recalls Select Cases of Its Cherry Ski Product

The Double Cola Company Recalls Select Cases of Its Cherry Ski Product

The Double Cola Company is recalling approximately 200 cases of its Cherry SKI product because they are incorrectly labeled. Only the Cherry SKI products with the new design are being recalled, which were delivered to the southern Illinois, Evansville, IN and Winchester, OH markets.

FDA - U.S. Food and Drug Administration

26-2-2018

Carnivore Meat Company Issues Voluntary Recall of “Vital Essentials Freeze-Dried Beef Nibblets Entrée for Dogs” Pet Food

Carnivore Meat Company Issues Voluntary Recall of “Vital Essentials Freeze-Dried Beef Nibblets Entrée for Dogs” Pet Food

Carnivore Meat Company of Green Bay, WI, is voluntarily recalling a limited amount, 73 cases, of “Vital Essentials Freeze-Dried Beef Nibblets Entrée for Dogs” pet food because the products have the potential to be contaminated with Salmonella. The recall includes only the product listed below.

FDA - U.S. Food and Drug Administration

26-2-2018

Progressive Laboratories, Inc. Issues Allergy Alert on Undeclared Milk in Product

Progressive Laboratories, Inc. Issues Allergy Alert on Undeclared Milk in Product

Progressive Laboratories, Inc., located at 3131 Story Road West, Irving, Texas 75038, USA, is voluntarily recalling Testosterzone, Thyroid Resilience, Xenesta Nuvive Men’s, and Xenesta Nuvive Women’s, because it may contain an undeclared allergen. People who have an allergy or severe sensitivity to milk could run the risk of serious or life-threatening allergic reaction if they consume these products.

FDA - U.S. Food and Drug Administration

25-2-2018

Lotte Int’l America Corp Issues Allergy Alert on Undeclared Peanut In "Kancho Choco Biscuit"

Lotte Int’l America Corp Issues Allergy Alert on Undeclared Peanut In "Kancho Choco Biscuit"

LOTTE Int’l America Corp. located in Los Angeles, CA is recalling its 1.48-ounce packages of "Kancho Choco Biscuit" manufactured by LOTTE Confectionery Co. Ltd. Korea because of findings of small amounts of peanut in the product and no peanut declaration.

FDA - U.S. Food and Drug Administration

24-2-2018

TruPet, LLC Issues Voluntary Recall of Certain "Treat Me Crunchy Beef Delight" Pet Treats

TruPet, LLC Issues Voluntary Recall of Certain "Treat Me Crunchy Beef Delight" Pet Treats

TruPet, LLC of Milford, OH, is voluntarily recalling a limited amount of Treat Me Crunchy Beef Delight, 2.5oz Pet treats because the products have the potential to be contaminated with Salmonella. The recall includes only the product listed below.

FDA - U.S. Food and Drug Administration

23-2-2018

DigiFab

DigiFab

Product approval information is indicated for Treatment of patients with life-threatening or potentially life-threatening digoxin toxicity or overdose.

FDA - U.S. Food and Drug Administration

23-2-2018

Labetalol Hydrochloride Injection by Hospira: Recall - Potential For Cracked Glass At Rim Surface Of Vials

Labetalol Hydrochloride Injection by Hospira: Recall - Potential For Cracked Glass At Rim Surface Of Vials

Cracked vials may result in a lack of sterility assurance. Use of or exposure to a non-sterile product may be associated with adverse events such as fever, chills, sepsis or invasive systemic infections in patients.

FDA - U.S. Food and Drug Administration

23-2-2018

La Pasta Inc/Heinen’s. Issues Allergy Alert on Undeclared Milk in Product Heinen’s Potato Gnocchi UPC# 02060141062

La Pasta Inc/Heinen’s. Issues Allergy Alert on Undeclared Milk in Product Heinen’s Potato Gnocchi UPC# 02060141062

La Pasta Inc. of Silver Spring, Maryland is recalling the private label Potato Gnocchi manufactured for Heinen’s supermarkets because it may contain undeclared milk. 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

22-2-2018

Seggiano USA, Inc. Issues Allergy Alert on Undeclared Tree Nuts

Seggiano USA, Inc. Issues Allergy Alert on Undeclared Tree Nuts

Seggiano USA, Inc. of Cheyenne, WY is voluntarily recalling Tuscan Kale Pesto mislabeled with Artichoke & Garlic labels because the labels do not declare tree nuts (cashews). Individuals who have allergies to tree nuts run the risk of a serious life-threatening allergic reaction if they consume the Tuscan Kale Pesto product. No incidents have been reported to date in connection with this issue.

FDA - U.S. Food and Drug Administration

22-2-2018

Snyder’s Lance Announces Voluntary Recall of a Limited Amount of 6.5 oz Emerald® Glazed Walnuts Due to Potential Presence of Undeclared Peanuts, Almonds, Cashews and Pecans

Snyder’s Lance Announces Voluntary Recall of a Limited Amount of 6.5 oz Emerald® Glazed Walnuts Due to Potential Presence of Undeclared Peanuts, Almonds, Cashews and Pecans

Emerald® Nuts is initiating a voluntary recall for a limited amount of its 6.5oz Glazed Walnuts product, distributed nationwide, due to the potential presence of undeclared peanuts, almonds, cashews and pecans in the product. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume this product

FDA - U.S. Food and Drug Administration

22-2-2018

Market of Choice Issues Allergy Alert on Undeclared Egg in Sezam Kale Salad

Market of Choice Issues Allergy Alert on Undeclared Egg in Sezam Kale Salad

Market of Choice of Eugene, Oregon is recalling Sezam Kale Salad because it may contain undeclared EGG. People who have an allergy or severe sensitivity to Egg run the risk of serious or life-threatening allergic reaction if they consume this product.

FDA - U.S. Food and Drug Administration

22-2-2018

Allergy Alert Issued by Sunneen Health Foods for Undeclared Pecan in Vegan Buffalo Chicken Bites

Allergy Alert Issued by Sunneen Health Foods for Undeclared Pecan in Vegan Buffalo Chicken Bites

Sunneen Health Foods is voluntarily recalling mislabeled Whole Foods Market Vegan Buffalo Chicken Bites sold at 13 Whole Foods Market stores in New York and New Jersey because the products contained tree nut (pecan) allergens that were not listed on the product label. The issue was discovered at the distribution center. People who have an allergy or severe sensitivity to pecans run the risk of serious or life-threatening allergic reaction if they consume these products.

FDA - U.S. Food and Drug Administration

20-4-2018

Biologicals regulatory framework proposed changes to start on 1 July 2018

Biologicals regulatory framework proposed changes to start on 1 July 2018

We are proposing changes to the Biologicals Regulatory Framework, including changes to autologous cell and tissue product regulation

Therapeutic Goods Administration - Australia

29-3-2018

BITE RELIEF SCHERER LABS (Benzocaine - 5.00%) Cream [Product Quest Mfg.]

BITE RELIEF SCHERER LABS (Benzocaine - 5.00%) Cream [Product Quest Mfg.]

Updated Date: Mar 29, 2018 EST

US - DailyMed

23-3-2018

CLOTRIMAZOLE Cream [Kareway Product, Inc.]

CLOTRIMAZOLE Cream [Kareway Product, Inc.]

Updated Date: Mar 23, 2018 EST

US - DailyMed

15-3-2018

Zinbryta (daclizumab)

Zinbryta (daclizumab)

Product withdrawn after overseas reports of inflammatory brain disorders

Therapeutic Goods Administration - Australia

6-3-2018

PURE-AID (Lidocaine, Menthol) Patch [Kareway Product, Inc.]

PURE-AID (Lidocaine, Menthol) Patch [Kareway Product, Inc.]

Updated Date: Mar 6, 2018 EST

US - DailyMed

1-3-2018

MAGIC STAMINA CLIMAX CONTROL (Benzocaine) Liquid [Product Max Group Inc]

MAGIC STAMINA CLIMAX CONTROL (Benzocaine) Liquid [Product Max Group Inc]

Updated Date: Mar 1, 2018 EST

US - DailyMed