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Teva Recalls Lot of Contaminated Topotecan 4 mg/4 mL Injection americanpharmaceuticalreview
July 05, 2021
Teva Pharmaceuticals has initiated a voluntary recall of lot 31328962B of Topotecan Injection 4 mg/4 mL (1 mg/mL), to the retail/institutional level in the United States.
Dr Reddy’s recalls 2,980 bottles of Atorvastatin Calcium tablets in US expresspharma
June 07, 2021
Dr Reddy’s Laboratories is recalling 2,980 bottles of Atorvastatin Calcium tablets in the US due to quality issues. Atorvastatin is indicated to lower cholesterol in the blood for adults and children over ten years of age.
Alembic Recalls Telmisartan Tablets 20 mg americanpharmaceuticalreview
April 01, 2021
Alembic Pharmaceuticals is voluntarily recalling one lot of Telmisartan Tablets, USP, 20 mg, packaged in 30-count bottles, Lot No. 1905005661 to the consumer level.
Zydus Recalls Acyclovir Sodium Injection, 50 mg/mL americanpharmaceuticalreview
March 29, 2021
Zydus Pharmaceuticals (USA) Inc. is voluntarily recalling four lots of Acyclovir Sodium Injection, 50 mg/mL, 10 mL and 20 mL vials, to the Hospital/User level after receiving several complaints of crystallization in vials.
Apotex Recalls Enoxaparin Sodium Injection americanpharmaceuticalreview
February 10, 2021
Apotex is voluntarily recalling two batches of Enoxaparin Sodium Injection, USP to consumer level due to a packaging error resulting in some syringes barrels containing 150 mg/mL markings (corresponding to 120 mg/0.8mL strength) instead of 100 mg/mL ...
Sun Pharma recalls 36,275 cartons of testosterone injection in the US for labelling error expresspharma
February 08, 2021
Sun Pharmaceutical is recalling 36,275 cartons of a drug used to treat low testosterone levels in the US market for incorrect labelling.
Precision Dose Recalls Paroex Chlorhexidine Gluconate Oral Rinse americanpharmaceuticalreview
January 13, 2021
Precision Dose, Inc. is voluntarily recalling all lots of Chlorhexidine Gluconate Oral Rinse USP, 0.12%, 15mL Unit Dose Cups bearing an expiration date from 1/31/2021 – 02/28/2022 to the consumer level. Precision Dose, Inc. was notified by the ...
DCGI asks state drug controllers to recall ulipristal acetate tablets from market expresspharma
November 19, 2020
The decision is based on the PRAC recommendations and reported cases of liver injury in the EU.
Bayshore Voluntarily Recalls Extended Release Metformin americanpharmaceuticalreview
August 25, 2020
The U.S. Food and Drug Administration (FDA) is alerting patients and health care professionals to Bayshore Pharmaceuticals’ voluntary recall of two lots of extended release (ER) metformin (one lot of 750 mg tablets and one lot of 500 mg tablets).
SCA Issues Recall of Heparin Sodium Compounded Products americanpharmaceuticalreview
August 24, 2020
SCA Pharmaceuticals (SCA) is voluntarily recalling 10 lots of Heparin Sodium to the hospital/user level. The compounded Heparin Sodium bag contains the undeclared preservative benzyl alcohol.

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