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Acid Reducer Original Strength FDA Alerts

The FDA Alerts below may be specifically about Acid Reducer Original Strength or relate to a group or class of drugs which include Acid Reducer Original Strength.

MedWatch Safety Alerts are distributed by the FDA and published by Drugs.com. Following is a list of possible medication recalls, market withdrawals, alerts and warnings.

Recent FDA Alerts for Acid Reducer Original Strength

Famotidine Injection, 20 mg/2 mL

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.]

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