FDA Drug Recalls

Recalls / Class II

Class IID-0174-2016

Product

PAPA/PGE1/PHENTO (30mg/10mg/1mg/ml) Injection, 5 mL and 10 mL vials, Rx, B & B Health Mart Pharmacy, Bellflower, CA

Affected lot / code info
5 ml --- 07062015@2, exp 1/2/2016 10 ml --- 06042015@4, exp 12/1/2015; 06052015@15, exp 12/2/2015; 07132015@3, exp 1/9/2016

Why it was recalled

Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility

Recalling firm

Firm
Pacific Healthcare, Inc dba B&B Pharmacy
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
10244 Rosecrans Ave, N/A, Bellflower, California 90706-2602

Distribution

Quantity
1-5 ml vial; 3-10 ml vials
Distribution pattern
CA and NJ

Timeline

Recall initiated
2015-10-07
FDA classified
2015-11-10
Posted by FDA
2015-11-18
Terminated
2016-04-07
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0174-2016. 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