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Safety Reports: Recall

Updated: March 22, 2022 8:08 PM

Real Time Reports

Recall notice

Pfizer Accuretic™, quinapril and hydrochlorothiazide; and quinapril HCl/hydrochlorothiazide tablets - recalled due to N-NitrosoQuinapril, USA

3 years ago •source fda.gov • details

Pfizer is voluntarily recalling Accuretic (quinapril HCl/hydrochlorothiazide) tablets distributed by Pfizer as well as two authorized generics distributed by Greenstone (quinapril and hydrochlorothiazide and quinapril HCl/ hydrochlorothiazide) to the patient (consumer/user) level due to the presence of a nitrosamine, N-nitroso-quinapril, above the Acceptable Daily Intake (ADI) level.… See more

#blood #pfizer #recall #drugs #unitedstates #vegetable #meat #ro-tel

Recalls Pfizer Accuretic™, quinapril and hydrochlorothiazide; and quinapril HCl/hydrochlorothiazide tablets... photo #1

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Recall notice

SYMJEPI Injection Pre-Filled Single-Dose Syringes - recalled due to potential clogging of the needle, USA

3 years ago •source fda.gov • details

Adamis Pharmaceuticals Corporation (Nasdaq: ADMP) is voluntarily recalling certain lots of SYMJEPI (epinephrine) Injection 0.15 mg (0.15 mg/0.3 mL) and 0.3 mg (0.3 mg/0.3 mL) Pre-Filled Single-Dose Syringes to the consumer level. The batches in the table below are being recalled due to the potential clogging of… See more

#recall #drugs #unitedstates #sub

Recalls SYMJEPI Injection Pre-Filled Single-Dose Syringes - recalled due to potential clogging of the needle... photo #1

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Recall notice

Sandoz Orphenadrine Citrate 100 mg Extended Release (ER) Tablets - recalled due to a Nitrosamine Impurity, USA

3 years ago •source fda.gov • details

Sandoz Inc. (“Sandoz”) is initiating a voluntary recall of 13 lots (listed below) of oral Orphenadrine Citrate 100 mg Extended Release (ER) Tablets to the consumer level. The presence of a nitrosamine (N-methyl-N-nitroso-2-[(2-methylphenyl)phenylmethoxy]ethanamine (NMOA or Nitroso-Orphenadrine)) impurity, which has the potential to be above the U.S. Food… See more

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

Recalls Sandoz Orphenadrine Citrate 100 mg Extended Release (ER) Tablets - recalled due to a Nitrosamine Imp... photo #1

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Recall notice

Ultra Healing Moisturizer - recalled due to a bacterium presence, USA

4 years ago •source fda.gov • details

Kao USA Inc. is asking consumers to check their Jergens® Ultra Healing Moisturizer 3 oz and 10 oz products to determine if it is part of a voluntary recall of the product. Select units of Jergens® Ultra Healing Moisturizer could show the presence of Pluralibacter gergoviae, a… See more

#cosmetics #recall #unitedstates

Recalls Ultra Healing Moisturizer - recalled due to a bacterium presence Kao USA Inc. is asking consumers to... photo #1

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Recall notice

Wilsons pet food products - recalled due to the presence of salmonella, UK

4 years ago •source data.food.gov.uk • details

Republic of Munchery Limited is recalling several pet feed products because of the presence of salmonella in one of the ingredients used to manufacture the products listed below.

The recalled products are:

- Wilsons Cold Pressed Haggis (2kg and 10kg), best before: 07 January 2023
- Wilsons… See more

#petfood #recall #unitedkingdom #beef #chicken #fish #salmon #turkey #pork

Recalls Wilsons pet food products - recalled due to the presence of salmonella Republic of Munchery Limited... photo #1

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Recall notice

Flowflex™ SARS-CoV-2 Antigen Rapid Test (Self-Testing) - recalled due to Unauthorized U.S. distribution, USA

4 years ago •source fda.gov • details

ACON Laboratories, Inc. (“ACON Laboratories”), the legal manufacturer of the “Flowflex™ COVID-19 Antigen Home Test” (FDA Emergency Use Authorization EUA210494), has identified the U.S. distribution of unauthorized, adulterated and misbranded counterfeit product having the trade name “Flowflex SARS-CoV-2 Antigen Rapid Test (Self-Testing).” ACON Laboratories is not importing… See more

#coronaviruscovid19 #recall #unitedstates #ro-tel

Recalls Flowflex™ SARS-CoV-2 Antigen Rapid Test (Self-Testing) - recalled due to Unauthorized U.S. distribut... photo #1

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Recall notice

Olympia Pharmacy Compounded Injectables - recalled due to products are out of specification, USA

4 years ago •source fda.gov • details

Olympia Pharmacy is voluntarily recalling 11 specific lots of Trimix Formulas F-9, T-105, SB-4, Sermorelin, Sincalide, Hydroxocobalamin, and NAD, compounded injectables to the consumer level. These compounded products were found to be out-of-specification.

The affected lots include the following lot numbers and expiration dates listed below. The… See more

#recall #drugs #unitedstates #sub

Recalls Olympia Pharmacy Compounded Injectables - recalled due to products are out of specification Olympia... photo #1

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Recall notice

Sneyd’s Wonderdog pet feed products- recalled due to the presence of salmonella, UK

4 years ago •source data.food.gov.uk • details

Sneyd’s Wonderfeeds Ltd is recalling several pet feed products because of the presence of salmonella in one of the ingredients used to manufacture.

The recalled products are:
- Sneyd’s Wonderdog Active Light (15Kg), Batch code: 5758, best before: 21 December 2022 06 January 2023
- Sneyd’s Wonderdog… See more

#dogfood #petfood #recall #unitedkingdom #salmon #bowl #specialk

Recalls Sneyd’s Wonderdog pet feed products- recalled due to the presence of salmonella Sneyd’s Wonderfeeds... photo #1

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Recall notice

Tennessee Technical Coatings Corp. Hand Sanitizer - recalled due to Product contains methanol, Tennessee, USA

4 years ago •source fda.gov • details

Tennessee Technical Coatings Corp. is voluntarily recalling all lots of HAND SANITIZER Isopropyl Alcohol Antiseptic 75% to the consumer/user level. FDA analysis has found the product to contain methanol. To date, Tennessee Technical Coatings Corp. has not received any reports of adverse events related to this recall.… See more

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

Recalls Tennessee Technical Coatings Corp. Hand Sanitizer - recalled due to Product contains methanol Tennes... photo #1

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Recall notice

Abbott Powder Infant Formula - recalled due to Cronobacter & Salmonella, USA

4 years ago •source fda.gov • details

*Update* March 07, 2022
EXPANDED: Abbott is voluntarily recalling one lot of Similac PM 60/40 (Lot # 27032K80 (can) / Lot # 27032K800 (case)) manufactured in Sturgis, Michigan. This is in addition to lots of Similac®, Alimentum® and EleCare® powder formula that were voluntarily recalled on Feb.… See more

#babyformula #recall #unitedstates #salmon #actii

Recalls Abbott Powder Infant Formula - recalled due to Cronobacter & Salmonella *Update* March 07, 2022
EXP... photo #1

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Safety Reports: Recall

Real Time Reports

Pfizer Accuretic™, quinapril and hydrochlorothiazide; and quinapril HCl/hydrochlorothiazide tablets - recalled due to N-NitrosoQuinapril, USA

SYMJEPI Injection Pre-Filled Single-Dose Syringes - recalled due to potential clogging of the needle, USA

Sandoz Orphenadrine Citrate 100 mg Extended Release (ER) Tablets - recalled due to a Nitrosamine Impurity, USA

Ultra Healing Moisturizer - recalled due to a bacterium presence, USA

Wilsons pet food products - recalled due to the presence of salmonella, UK

Flowflex™ SARS-CoV-2 Antigen Rapid Test (Self-Testing) - recalled due to Unauthorized U.S. distribution, USA

Olympia Pharmacy Compounded Injectables - recalled due to products are out of specification, USA

Sneyd’s Wonderdog pet feed products- recalled due to the presence of salmonella, UK

Tennessee Technical Coatings Corp. Hand Sanitizer - recalled due to Product contains methanol, Tennessee, USA

Abbott Powder Infant Formula - recalled due to Cronobacter & Salmonella, USA

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