FDA Drug Recalls

Recalls / Class II

Class IID-0941-2020

Product

B-COMPLEX 110 INJECTABLE, For IV, IM, SC Use, Refrigerate, 30 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0212-3

Affected lot / code info
Lot #: 07022019+52584, 07022019+52579, Exp 3/29/2020; 08012019+52780, 08012019+52782, Exp 4/28/2020; 11262019+53288, Exp 8/23/2020

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-0941-2020. 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