Zydus Lifesciences Limited – 08/13/2025

FDA provides resources on pharmaceutical quality topics, including information on regulations, guidance documents, and compliance programs.

Center Valley, Pa., (December 5, 2025)-Olympus Corporation today announced a voluntary medical device corrective action for its Single-Use Ligating Device (“Polyloop”) following identification of a potential safety issue.

Gusto Group Inc. of Paterson, NJ is recalling [Klong Kone] Shrimp Paste (Klong Kone) ‘454 G. (1 LBS)’ and ‘910 G. (2 LBS)’ because it has the potential to be contaminated with elevated levels of lead. Short term exposures to very low levels of lead may not elicit any symptoms. It is possible that

Find answers to the most asked questions about medication health fraud and how to identify scams when buying products.

The Compounding Quality Center of Excellence’s free in-person training programs target outsourcing facility staff and offer continuing education credits. The training will open for state regulators and pharmacy compounders if space is available.

Learn more about FDA’s Postmarketing Requirements and Commitments Searchable Database.