FDA recall record

Famotidine Injection, USP, 20 mg per 2 mL (10 mg per mL), 2 mL vials recall — FDA D-0182-2026

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

Class Iclassification
D-0182-2026official record ID
Dec 3, 2025report date

Recall record at a glance

Official recordD-0182-2026
CategoryDrug Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmFresenius Kabi USA, LLC
Report dateDec 3, 2025
Recall initiation dateNov 6, 2025
Quantity2,199,850 vials
LocationLake Zurich, IL, United States

Official product description

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).

Why the product was recalled

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

Distribution information

Nationwide within the United States as well as AK, HI, and PR.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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