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The UK Medicines and Healthcare products Regulatory Agency (MHRA) has highlighted a Class 2 recall of one batch of Fingolimod Zentiva 0.5 mg Capsules after shelf-life testing identified a potential risk of metal-particle contamination. Zentiva UK Pharma Limited is recalling
Vitruvias Therapeutics is voluntarily recalling one nationwide lot of Thyroid Tablets, USP 30 mg after testing confirmed potential superpotency. The affected lot 504950 was distributed across the United States between January 31 and September 30, 2025. FDA published the company
India’s Central Drugs Standard Control Organisation (CDSCO) has flagged 40 batches of medicines and healthcare products as Not of Standard Quality (NSQ) in its July 2026 surveillance results. The samples failed pharmacopoeial or manufacturer specifications across tests including sterility and
The U.S. Food and Drug Administration (FDA) has issued a Warning Letter to ABS Corporation, a veterinary drug manufacturer in Omaha, Nebraska, after a January 2026 inspection identified significant CGMP violations involving OOS investigations, incoming component testing, and process validation.
Shilpa Medicare is voluntarily recalling more than 27,000 vials of Pemetri RTU chemotherapy drug in the United States after market complaints reported green to dark-green discoloration in certain vials. The nationwide action involves two strengths and has been classified by