FDANovember 6, 2025drug

Famotidine Injection, USP, 20 mg per 2 mL (10 mg per mL), 2 mL vials, Rx only, Fresenius Kabi USA, LLC, NDC 63323-739-11 (unit of use), 63323-739-12 (unit of sale).

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.

What to do

FDA enforcement status: Ongoing

Brands named

fresenius kabifresenius

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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