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Safety Reports: Recall

Updated:

Real Time Reports

Recall notice

ByHeart Whole Nutrition Infant Formula - recalled due to Cronobacter Akasaki, USA

3 years ago •source fda.gov • details

The product being recalled is ByHeart Whole Nutrition Infant Formula, Milk Based Powder with Iron for 0-12 Months in 24 oz containers. The formula under voluntary recall was distributed directly to consumers in the U.S. and can be identified by the number on the bottom of the… See more

#blood #recall #unitedstates #milk #actii

Recalls ByHeart Whole Nutrition Infant Formula - recalled due to Cronobacter Akasaki The product being recal... photo #1
312   Comments Comment

Recall notice

Cranberry Sweets Mint Meltaways - recalled due to allergens, USA

3 years ago •source fda.gov • details

Cranberry Sweets & More of Coos Bay, Oregon is voluntarily recalling its 4 and 8 ounce packages of "Mint Meltaways" candies 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.… See more

#peanutallergy #recall #unitedstates #sub #butter #peanuts #peanutbutter

Recalls Cranberry Sweets Mint Meltaways - recalled due to allergens Cranberry Sweets & More of Coos Bay, Ore... photo #1
312   Comments Comment

Recall notice

TUMS Peppermint Regular Strength tablets - recalled due to contamination, Canada

3 years ago •source recalls-rappels.canada.ca • details

GlaxoSmithKline Consumer Healthcare ULC is recalling one lot of TUMS Peppermint Regular Strength tablets after some tablets were found to contain fragments of fibreglass and other material, including paper and aluminum foil. The product is sold in a package of three rolls containing 12 tablets each, and… See more

#drugs #recall #canada #pepper #roll

Recalls TUMS Peppermint Regular Strength tablets - recalled due to contamination GlaxoSmithKline Consumer He... photo #1
87   Comments Comment

Recall notice

The Laundress products - safety notice to stop using them due to elevated levels of bacteria, USA

3 years ago •source thelaundress.com • details

The Laundress New York issued a safety notice to stop using all their products due to the potential presence of elevated levels of bacteria in some of its products. These Bacteria identified in product testing are so-called "opportunistic" pathogens, including Pseudomonas, which occur naturally in water and… See more

#recall #unitedstates

Recalls The Laundress products - safety notice to stop using them due to elevated levels of bacteria The Lau... photo #1
312   Comments Comment

Recall notice

Exela Sodium Bicarbonate Injection vial - recalled due to vial breakage, USA

3 years ago •source fda.gov • details

Exela Pharma Sciences, LLC, (Exela) is expanding their recall, adding fourteen (14) lots to the ongoing voluntary recall of forty-nine (49) lots of Sodium Bicarbonate Injection, USP, 8.4%, 50 mEq/50 mL vial, 20-count carton. A total of 63 lots are now being recalled to the consumer level.… See more

#recall #drugs #unitedstates #corn #sub

Recalls Exela Sodium Bicarbonate Injection vial - recalled due to vial breakage Exela Pharma Sciences, LLC,... photo #1
312   Comments Comment

Recall notice

Marijuana products cultivated by PP Wellness - recalled due to possible Aspergillus contamination, Arizona, USA

3 years ago •source azdhs.gov • details

The Arizona Department of Health Services (ADHS) announced the recall of specific marijuana products cultivated by PP Wellness due to possible contamination with Aspergillus, a fungus that can cause allergic reactions or infection, usually in people already sick with something else. These products were sold at multiple… See more

#marijuana #recall #otherallergens #arizona #unitedstates #juice

Recalls Marijuana products cultivated by PP Wellness - recalled due to possible Aspergillus contamination Th... photo #1
114   Comments Comment

Recall notice

Healthy Sense and People’s Choice Daily multi vitamin with Iron and Women’s daily vitamin with iron - recalled due to due to components lower than declared, USA

3 years ago •source fda.gov • details

Mason Vitamins Inc. has issued a nationwide voluntary recall of the specific lot of Healthy Sense Daily Multiple with Iron and People’s Choice Women's Daily Vitamins with Iron due to Vitamin A, Vitamin B12, Vitamin C, Vitamin E and Pantothenic Acid amounts being lower than the declared… See more

#drugs #recall #unitedstates #healthychoice #ro-tel

Recalls Healthy Sense and People’s Choice Daily multi vitamin with Iron and Women’s daily vitamin with iron... photo #1
312   Comments Comment

Recall notice

Holland & Barrett is recalling soya lecithin soft gel capsules - recalled due to undeclared peanuts, UK

3 years ago •source food.gov.uk • details

Holland & Barrett is recalling soya lecithin soft gel capsules because they contain peanuts which are not mentioned on the label. This means the product is a possible health risk for anyone with an allergy to peanuts.

The recalled products are:
- Ultra Soya Lecithin 1200mg (50… See more

#peanutallergy #soyallergy #recall #unitedkingdom #soy #peanuts

Recalls Holland & Barrett is recalling soya lecithin soft gel capsules - recalled due to undeclared peanuts... photo #1
158   Comments Comment

Recall notice

Adam’s Polishes Hand sanitizer - recalled due to presence of methanol, USA

3 years ago •source fda.gov • details

Thornton, Colorado, Adam’s Polishes, LLC is voluntarily recalling lot 133475 of Adam’s Polishes Hand Sanitizer to the consumer level. FDA testing has found this lot to contain undeclared methanol. Adam’s Polishes is recalling 19 other lots in an abundance of caution. The hand sanitizer was distributed nationwide… See more

#handsanitizer #recall #unitedstates #sub #ro-tel

Recalls Adam’s Polishes Hand sanitizer - recalled due to presence of methanol Thornton, Colorado, Adam’s Pol... photo #1
312   Comments Comment

Recall notice

Insulet Corporation Omnipod DASH Personal Diabetes Managers - recalled due to battery issue, USA

3 years ago •source fda.gov • details

Insulet Corporation (NASDAQ: PODD) (Insulet or the Company), announced on October 17, 2022, a Medical Device Correction for all Omnipod DASH® Personal Diabetes Managers (PDMs) distributed globally. This action was taken voluntarily with the knowledge of the FDA and other regulatory agencies. Insulet received reports from Omnipod… See more

#recall #medicaldevices #unitedstates

Recalls Insulet Corporation Omnipod DASH Personal Diabetes Managers - recalled due to battery issue Insulet... photo #1
312   Comments Comment

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