FDA Drug Recalls

Recalls / Class II

Class IID-0951-2020

Product

Dexamethasone (LA) Injectable Suspension, DEXAMETHASONE LA [10ML] 16MG INJ SUSP, For IM, IA Use, Shake Well, 10 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0630-1

Affected lot / code info
Lot #: 10022019+53002, Exp 10/1/2020

Why it was recalled

Lack of Assurance of Sterility

Recalling firm

Firm
Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical
Notification channel
Press Release
Type
Voluntary: Firm initiated
Address
1990 Westwood Blvd Ste 135, N/A, Los Angeles, California 90025-4650

Distribution

Quantity
N/A
Distribution pattern
U.S.A. Nationwide and Puerto Rico, Barbados and Dominican Republic

Timeline

Recall initiated
2020-01-15
FDA classified
2020-03-05
Posted by FDA
2020-03-11
Terminated
2023-12-07
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0951-2020. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls