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Nearly 40,000 Clear Eyes Bottles Recalled Over Sterility Concerns

The FDA classified the voluntary recall as Class II to signal regulatory concern about eye‑drop sterility; consumers are advised to stop using or return affected bottles.

Nearly 12 Million Rohto Eye Drop Cartons Recalled Over Sterility Concerns

FDA Says Metals Found in Tampons Are Not at Harmful Levels

FDA Allows Zyn to Be Marketed as Lower Risk Than Cigarettes

Massachusetts Med-Spa Owner Pleads Guilty to Using Counterfeit Botox and Fillers

FDA Eases Oversight of Wearables and Clinical Decision Support in Final Guidance

ByHeart Recalls All U.S. Infant Formula as Botulism Investigation Expands

FDA Halts Sales of Unapproved Ingestible Fluoride for Children 3 and Under

FDA Hears Final Testimony on Removing Prescription Fluoride Supplements