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Safety Reports: Recall

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

11 months 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

Aactive D3 supplements recalled due of excess levels of Vitamin D3, UK

1 year ago •source data.food.gov.uk • details

TriOn Pharma is recalling two food supplement products. Aactive D3 Drops and Aactive D3 Solution because they contain higher levels of vitamin D3 than written on the label.

Product details:
- Product Name: Aactive D3 2,000iu/ml Oral Drops, Pack size: (20ml), Batch code: LS23317, Best before: November… See more

#recall #supplement #unitedkingdom

Recalls Aactive D3 supplements recalled due of excess levels of Vitamin D3 TriOn Pharma is recalling two foo... 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

#recall #drugs #unitedstates

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

#drugs #recall #unitedstates

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

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Recall notice

Force Forever Dietary Supplement - recalled due to diclofenac and dexamethasone, USA

1 year ago •source fda.gov • details

GNMART INC is voluntarily recalling all lots of Force Forever for joint Pain to the consumer level. FDA analysis has found product to contain undeclared Diclofenac and Dexamethasone. The product was distributed nationwide via the internet at gnmart.com External Link Disclaimer.

Risk Statement: Diclofenac is a non-steroidal… See more

#recall #dietarysupplements #unitedstates

Recalls Force Forever Dietary Supplement - recalled due to diclofenac and dexamethasone GNMART INC is volunt... 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

Umary Hyaluronic Acid tablets - recalled due to diclofenac and omeprazole, USA

1 year ago •source fda.gov • details

MXBBB is voluntarily recalling 1 lot of UMARY ACID HYALURONIC to the consumer level. The products have been found to have omeprazole and diclofenac. FDA laboratory analysis confirmed that Umary contains diclofenac and omeprazole. UMARY has been distributed across the USA Via Amazon.

Risk Statement: The product… See more

#dietarysupplements #recall #amazon #unitedstates

Recalls Umary Hyaluronic Acid tablets - recalled due to diclofenac and omeprazole MXBBB is voluntarily recal... 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

#recall #drugs #unitedstates

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

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Safety Reports: Recall

Real Time Reports

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

Aactive D3 supplements recalled due of excess levels of Vitamin D3, UK

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

Force Forever Dietary Supplement - recalled due to diclofenac and dexamethasone, USA

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

Umary Hyaluronic Acid tablets - recalled due to diclofenac and omeprazole, USA

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

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