Fresenius Kabi Usa, LLC — Famotidine Injection recall — Check with your pharmacist

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Fresenius Kabi Usa, LLC

Check with your pharmacist

Do not stop taking a prescribed medicine on your own — ask your pharmacist for a replacement pack today.

Class I

The FDA’s most serious category — a reasonable probability of serious harm or death.
Refunds don't require a receipt, and you don't need proof of purchase.
FDA status: Ongoing.

What was recalled

Source: FDA · synced 29 Jul 2026 13:14

Check with your pharmacist Filed 2025-12-03

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

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).

Check these codes: Lot #: 6133156, 6133194, Exp Date: 08/2026; 6133388, Exp Date: 10/2026.

2,199,850 vials · distributed nationwide within the united states as well as ak, hi, and pr. Recall D-0182-2026 on FDA.gov ↗

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