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Quality Control

Product Recalls Product Safety Regulatory Compliance Inspection Procedures FDA Regulations Ascend Laboratories Recalls Sresan Pharma Product Contamination Packaging Errors

Manufacturer Recalls Four Lots of Generic Zyrtec Over Possible Ranitidine Contamination

The limited recall warns ranitidine cross‑contamination could cause life‑threatening allergic reactions for people who are sensitive to ranitidine.

FDA Classifies Chlorthalidone Recall as Class II

Nationwide Recall of 25 mg Chlorthalidone Covers 11,460 Bottles

FDA Eases CMC Rules for Cell and Gene Therapies to Speed Development

Doctor’s Wife Arrested as Seventh Accused in Madhya Pradesh Cough Syrup Deaths Case

Teva, Amerisource Pull 580,000+ Prazosin Bottles as FDA Flags Nitrosamine Contamination

Ascend Recalls 141,984 Bottles of Generic Atorvastatin Over Dissolution Failures

Coldrif Maker’s Owner Arrested as Tests Show Extreme Diethylene Glycol in Syrup

Owner Arrested in Coldrif Cough Syrup Deaths as Tamil Nadu Launches Criminal Case

ANMAT Suspends Production at Sant Gall Friburg’s Buenos Aires Plant Over GMP Breaches