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U.S. Department of Health and Human Services

Safety

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Famotidine Injection, 20 mg/2 mL

Audience: Pharmacists and other healthcare professionals

Bedford Laboratories and FDA notified healthcare professionals of the voluntary recall of one lot of Famotidine Injection, 20 mg/2 mL (NDC 55390-029-10), Lot# 609336, exp. 04/06, due to a lack of sterility assurance. This prescription product was distributed in August 2004 throughout the United States to wholesalers and distributors, who further distributed the product to hospitals.

[April 29, 2005 - Press Release - Bedford Laboratories, Inc.]