FDA Drug Recalls

Recalls / Class II

Class IID-1306-2015

Product

SIU-Tri-Mix 20/1 mg/10 mcg/mL, Rx Only, 10 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 13452-2913-85

Affected lot / code info
Lot #: 05202015@14, BUD 11/16/2015

Why it was recalled

Lack of Assurance of Sterility: Due to lack of documentation of proper environmental monitoring during the time in which the medication was produced.

Recalling firm

Firm
The Apothecary Shoppe LLC
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
6136 E 51st St, N/A, Tulsa, Oklahoma 74135-7704

Distribution

Quantity
10 mL
Distribution pattern
Oklahoma

Timeline

Recall initiated
2015-06-26
FDA classified
2015-08-06
Posted by FDA
2015-08-12
Terminated
2017-02-17
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1306-2015. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.