FDA Drug Recalls

Recalls / Class II

Class IID-0179-2016

Product

PAPA/PGE1/PHENTO (35mg/12mcg/1.5mg/ml), Injection, 10 mL vial, Rx, B & B Health Mart Pharmacy, Bellflower, CA

Affected lot / code info
08032015@4, exp 1/30/2016

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 vial
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-0179-2016. 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