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Safety Reports: Recall

Updated: November 24, 2022 5:22 PM

Real Time Reports

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 #otherallergens #recall #arizona #unitedstates #juice

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

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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

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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

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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

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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

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Recall notice

Gibeck® and Iso-Gard® Bacterial and viral filters - recalled due to Bacterial and viral filters, USA

3 years ago •source fda.gov • details

Teleflex Incorporated (NYSE: TFX), a leading global provider of medical technologies for critical care and surgery, has announced a worldwide recall of affected lots of the below-referenced Gibeck® Iso-Gard® Filter products. The Gibeck® Iso-Gard® Filter is a bacterial and viral filter, intended for connection to respiratory equipment… See more

#recall #medicaldevices #unitedstates

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Recall notice

Mighty Bliss Electric Heating Pad - recalled due to product safety concerns, USA

3 years ago •source fda.gov • details

Whele LLC, of Boston, MA, is voluntarily recalling its Mighty Bliss Electric Heating Pad, due to product safety concerns. Use of this product may lead to burns, mild shocks, or rashes/irritation. Product was sold via Amazon.com and Walmart.com. We received 286 complaints between July 2021 to September… See more

#recall #amazon #walmart #medicaldevices #unitedstates #sub #ro-tel

Recalls Mighty Bliss Electric Heating Pad - recalled due to product safety concerns Whele LLC, of Boston, MA... photo #1

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Recall notice

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

3 years ago •source fda.gov • details

Exela Pharma Sciences, LLC, (Exela) is voluntarily recalling 49 lots of Sodium Bicarbonate Injection, USP, 8.4%, 50 mEq/50 mL vial, 20count carton, to the consumer level. Product was distributed nationwide to wholesalers, distributors, and other customers between December 16, 2021 and August 10, 2022.

Risk Statement: The… See more

#recall #drugs #unitedstates #corn #sub

Recalls Exela & Civica Sodium Bicarbonate Injection - recalled due to vial breakage Exela Pharma Sciences, L... photo #1

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Recall notice

Golden State Medical Supply Clopidogrel & Atenolol - recalled due to label mix-up, USA

3 years ago •source fda.gov • details

Golden State Medical Supply, Incorporated (GSMS, Inc.) - Camarillo, CA has initiated a voluntary recall of the products listed in the table below because a report was received that a bottle containing Clopidogrel 75mg Tablets produced with lot# GS046745 was mislabeled as Atenolol 25mg Tablets. This voluntary… See more

#blood #recall #drugs #unitedstates

Recalls Golden State Medical Supply Clopidogrel & Atenolol - recalled due to label mix-up Golden State Medic... photo #1

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Recall notice

My Stellar Lifestyle Wonder Pill Capsules - recalled due to undeclared tadalafil, USA

3 years ago •source fda.gov • details

Proper Trade LLC/My Stellar Lifestyle is voluntarily recalling Wonder Pill lot 20210912 and lot 31853-501, expiry 09/24, packaged in 10-count blisters co-packaged in a carton and in 60-count bottles to the consumer level. Proper Trade LLC/My Stellar Lifestyle was notified by Amazon that laboratory analysis has found… See more

#blood #recall #drugs #unitedstates #sub #ro-tel

Recalls My Stellar Lifestyle Wonder Pill Capsules - recalled due to undeclared tadalafil Proper Trade LLC/My... photo #1

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Safety Reports: Recall

Real Time Reports

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

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

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

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

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

Gibeck® and Iso-Gard® Bacterial and viral filters - recalled due to Bacterial and viral filters, USA

Mighty Bliss Electric Heating Pad - recalled due to product safety concerns, USA

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

Golden State Medical Supply Clopidogrel & Atenolol - recalled due to label mix-up, USA

My Stellar Lifestyle Wonder Pill Capsules - recalled due to undeclared tadalafil, USA

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