Famotidine: 10 recalls on record

Recalled by 1 agency: FDA (10).

First recall on record: September 3, 2014. Most recent: September 9, 2026.

Risk classification: Class I: 1 · Class II: 5 · Class III: 4

Most recent recalls

DateAgencyProduct
September 9, 2026FDAFamotidine Injection in Sodium Chloride Injection, 20 mg, 50 mL in GALAXY Single Dose Con…D-0809-2026
December 3, 2025FDAFamotidine Injection, USP, 20 mg per 2 mL (10 mg per mL), 2 mL vials, Rx only, Fresenius …D-0182-2026
July 26, 2023FDAFamotidine Tablets, USP, 20mg, 200-count bottle within a carton, Distributed by: Glenmark…D-0939-2023
March 10, 2021FDAFamotidine Tablets USP 40mg, 1,000-count bottles, Rx only, Distributed by: Aurobindo Phar…D-0290-2021
July 29, 2020FDAFamotidine Injection, USP, 20 mg/2mL, 2 mL vial, Rx only, Single Dose Vial, For Intraveno…D-1392-2020
October 18, 2017FDAFamotidine tablets, 10 mg, packaged in 30-count bottle, OTC, labeled as a) CVS Pharmacy A…D-0009-2018
September 13, 2017FDAFamotidine for Oral Suspension USP, 40 mg/5 mL, 50 mL bottle, Rx only, Manufactured for: …D-1127-2017
August 9, 2017FDAFamotidine Tablets USP, 20 mg, 100 count bottles, Rx only, Manufactured For: TEVA PHARMA…D-1056-2017
December 17, 2014FDAFamotidine Injection 20 mg, Rx Only, GALAXY Single Dose Container, Code 2G3424, Sterile N…D-0293-2015
September 3, 2014FDAFamotidine for Oral Suspension, USP 40 mg/5 mL, Rx Only, Cherry-Banana-Mint Flavored, Not…D-1484-2014

Questions about this brand

How many recalls does Famotidine have?
Recalert has 10 U.S. recalls on record for Famotidine, published between September 3, 2014 and September 9, 2026.
What was the most recent Famotidine recall?
FDA recall D-0809-2026, published September 9, 2026: Famotidine Injection in Sodium Chloride Injection, 20 mg, 50 mL in GALAXY Single Dose Container, Rx Only, Sterile Nonpyrogenic, Baxter International Inc., Baxter Healthcare Corporation, Deerfield, IL…
Which agencies have recalled Famotidine products?
Famotidine products appear in recalls from: FDA (10).

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