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Safety Reports: Drugs

Updated: January 24, 2025 3:01 PM

Real Time Reports

Recall notice

Phenylephrine hydrochloride Injection, USP, 10 mg/ mL recalled due to Potential Foreign Material, USA

1 year ago •source fda.gov • details

Provepharm Inc. is voluntarily recalling lot number 24020027; Expiry Date December 2025 of Phenylephrine hydrochloride Injection, USP, 10 mg/ mL (Pharmacy Bulk Package) at the hospital/institutional level. This recall was initiated based on a customer complaint from a pharmacy after observing a visible black particulate matter found… See more

#recall #drugs #unitedstates

Recalls Phenylephrine hydrochloride Injection, USP, 10 mg/ mL recalled due to Potential Foreign Material Pro... photo #1

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Recall notice

Astellas Tacrolimus and Tacrolimus Extended-Release capsules - recalled due to Bottles may contain empty capsules., USA

1 year ago •source fda.gov • details

Astellas Pharma US, Inc. is voluntarily recalling one lot of PROGRAF® 0.5mg (tacrolimus) and one lot of ASTAGRAF XL® 0.5mg (tacrolimus extended-release) capsules to the consumer level. These products are being recalled because bottles may contain empty capsules. The product was distributed nationwide to wholesale and retail… See more

#recall #drugs #unitedstates

Recalls Astellas Tacrolimus and Tacrolimus Extended-Release capsules - recalled due to Bottles may contain e... photo #1

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Recall notice

Systane Lubricant Eye Drugs - recalled due to Fungal Contamination, USA

1 year ago •source fda.gov • details

Alcon Laboratories is voluntarily recalling one (1) lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count to the consumer level. Alcon evaluated a consumer complaint of foreign material observed inside a sealed single use vial and determined the material to be fungal in… See more

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Recalls Systane Lubricant Eye Drugs - recalled due to Fungal Contamination Alcon Laboratories is voluntarily... photo #1

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Recall notice

Par Pharmaceutical Adrenalin® Chloride Solution recalled due to an unapproved drug, USA

1 year ago •source fda.gov • details

Endo USA, Inc., is voluntarily recalling all lots within expiry of Adrenalin® Chloride Solution (EPINEPHrine nasal solution, USP) 30mg/30mL (1mg/mL) 30 mL vials, to the consumer level. This product, which pre-dates the 1938 Federal Food, Drug & Cosmetic Act, was never submitted for approval by the FDA,… See more

#recall #drugs #unitedstates

Recalls Par Pharmaceutical Adrenalin® Chloride Solution recalled due to an unapproved drug Endo USA, Inc., i... photo #1

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Recall notice

Fouzee SugarLin Herbal Dietary Supplement recalled due to Metformin and Glyburide, USA

1 year ago •source fda.gov • details

Shoppers-Plaza is voluntarily recalling all lots of Fouzee Sugarlin Herbal Formula capsules to the consumer level. Fouzee Sugarlin Herbal Formula capsules is an unapproved new drug for which safety and efficacy have not been established and, therefore, subject to recall. This product was promoted and sold nationwide… See more

#recall #drugs #unitedstates

Recalls Fouzee SugarLin Herbal Dietary Supplement recalled due to Metformin and Glyburide Shoppers-Plaza is... photo #1

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Recall notice

Buy-herbal.com Dietary Supplement Capsules - recalled due to unapproved drug, USA

1 year ago •source fda.gov • details

Buy-herbal.com is voluntarily recalling all lots within expiry of Nhan Sam Tuyet Lien Truy Phong Hoan Capsules to the consumer level. FDA analysis has found these products to contain undeclared Furosemide, Dexamethasone and Chlorpheniramine.

Furosemide was found at 5.24 mg/g or 1.84 mg/capsule. Dexamethasone was found at… See more

#recall #drugs #unitedstates

Recalls Buy-herbal.com Dietary Supplement Capsules - recalled due to unapproved drug Buy-herbal.com is volun... photo #1

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Recall notice

Par Pharmaceutical Clonazepam Orally Disintegrating Tablets recalled due to mislabeled, USA

1 year ago •source fda.gov • details

Endo, Inc. announced today that one of its operating subsidiaries, Endo USA, Inc., is expanding its previously announced voluntary recall of Clonazepam Orally Disintegrating Tablets, USP (C-IV) due to potential product carton strength mislabeling. Specifically, Endo's ongoing investigation has identified the possibility that the Clonazepam product lots… See more

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Recalls Par Pharmaceutical Clonazepam Orally Disintegrating Tablets recalled due to mislabeled Endo, Inc. an... photo #1

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Recall notice

AK Forte Dietary Supplement - recalled due to unapproved drug, USA

1 year ago •source fda.gov • details

C&A Naturistics is voluntarily recalling all lots of AK Forte, 400 mg tablets, to the consumer level. FDA analysis has found the product to be tainted Diclofenac, Dexamethasone, and Methocarbamol. Products containing diclofenac, dexamethasone, and methocarbamol cannot be marketed as dietary supplements. AK Forte tablets is an… See more

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Recalls AK Forte Dietary Supplement - recalled due to unapproved drug C&A Naturistics is voluntarily recalli... photo #1

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Recall notice

Staska Pharmaceuticals Ascorbic Acid Solution - recalled due to glass particulates, USA

1 year ago •source fda.gov • details

Staska Pharmaceuticals, INC. is voluntarily recalling 1 lot of Ascorbic Acid Solution for Injection to the user level. This is due to the presence of glass particulates in one lot of vials used in the production of this batch. The product was distributed nationwide in USA to… See more

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Recalls Staska Pharmaceuticals Ascorbic Acid Solution - recalled due to glass particulates Staska Pharmaceut... photo #1

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Recall notice

Gilead Veklury (remdesivir) for Injection - recalled due to presence of Glass Particle, USA

1 year ago •source fda.gov • details

Gilead Sciences, Inc. issued a voluntary recall of one lot of Veklury® (remdesivir) for Injection to the consumer level. The product was distributed nationwide in the United States, beginning 16 July 2024

Risk Statement: The administration of an injectable product that contains glass particles may result in… See more

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Recalls Gilead Veklury (remdesivir) for Injection - recalled due to presence of Glass Particle Gilead Scienc... photo #1

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Safety Reports: Drugs

Real Time Reports

Phenylephrine hydrochloride Injection, USP, 10 mg/ mL recalled due to Potential Foreign Material, USA

Astellas Tacrolimus and Tacrolimus Extended-Release capsules - recalled due to Bottles may contain empty capsules., USA

Systane Lubricant Eye Drugs - recalled due to Fungal Contamination, USA

Par Pharmaceutical Adrenalin® Chloride Solution recalled due to an unapproved drug, USA

Fouzee SugarLin Herbal Dietary Supplement recalled due to Metformin and Glyburide, USA

Buy-herbal.com Dietary Supplement Capsules - recalled due to unapproved drug, USA

Par Pharmaceutical Clonazepam Orally Disintegrating Tablets recalled due to mislabeled, USA

AK Forte Dietary Supplement - recalled due to unapproved drug, USA

Staska Pharmaceuticals Ascorbic Acid Solution - recalled due to glass particulates, USA

Gilead Veklury (remdesivir) for Injection - recalled due to presence of Glass Particle, USA

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