FDA Drug Recalls

Recalls / Class II

Class IID-1341-2015

Product

Chorionic Gonadotropin/ Hydroxocobalamin Lyophilized Powder Injectable, 10,000 UNITS/ 5000 mcg per vial, Rx Only, Manufactured by Park Compounding, Irving, CA

Affected lot / code info
Lot # 120322014@1B, Exp 05/15

Why it was recalled

Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.

Recalling firm

Firm
South Coast Specialty Compounding, Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
9257 Research Dr, N/A, Irvine, California 92618-4286

Distribution

Quantity
337 vials (112 prescriptions)
Distribution pattern
Nationwide.

Timeline

Recall initiated
2015-04-23
FDA classified
2015-09-02
Posted by FDA
2015-09-09
Terminated
2016-05-31
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1341-2015. 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