RecallRadar

Famotidine Device Recalls

View recent famotidine recall notices and find official safety instructions and remedies.

All BrandsFamotidineAppleSamsungGoogleSonyMicrosoftDell
Lot #: 6133156, 6133194, Exp Date: 08/2026; 6133388, Exp Date: 10/2026.medium

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).

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

Lot #: 6133156, 6133194, Exp Date: 08/2026; 6133388, Exp Date: 10/2026.
November 6, 2025
1
Active Recalls
0
High Priority
1
Device Types Affected

Own an Famotidine device?

Register your devices and we'll notify you instantly when a new recall is announced.

Register Your Devices
Famotidine Device Recalls | RecallRadar