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Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical recalls Alprostadil (prostaglandin E1) 80 MCG/ML Injectable, For Intracavernosal Use, Freeze, 2.5 mL Multi-dose Vial, Rx only, A

Recalled March 11, 2020 · FDA recall D-0936-2020 · Fusion IV Pharmaceuticals, Inc.

Hazard
Lack of Assurance of Sterility · FDA Class II
Units
N/A
Sold at
U.S.A. Nationwide and Puerto Rico, Barbados and Dominican Republic

Description

Lack of Assurance of Sterility

Product
Alprostadil (prostaglandin E1) 80 MCG/ML Injectable, For Intracavernosal Use, Freeze, 2.5 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0543-2
Manufacturer(s)
Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical recalls Alprostadil (prostaglandin E1) 80 MCG/ML Injectable, For Intracavernosal Use, Freeze, 2.5 mL Multi-dose Vial, Rx only, A | RecallWatchUSA