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Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical recalls BETAMETHASONE ACETATE/BETAMETHASONE (PF) Injectable Suspension, Betamethasone Acetate/Betamethasone (PF) CMC [2ML] 6MG/M

Recalled March 11, 2020 · FDA recall D-0942-2020 · 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
BETAMETHASONE ACETATE/BETAMETHASONE (PF) Injectable Suspension, Betamethasone Acetate/Betamethasone (PF) CMC [2ML] 6MG/ML INJ SUSP, For IM, IA, IT Use, Shake Well. Preservative Free. Discard Unused Portion, 2 mL Single-use Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0620-2
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 BETAMETHASONE ACETATE/BETAMETHASONE (PF) Injectable Suspension, Betamethasone Acetate/Betamethasone (PF) CMC [2ML] 6MG/M | RecallWatchUSA