FDA Drug Recalls

Recalls / Class II

Class IID-1311-2015

Product

SIU-Tri-Mix 30/1/20 Injectable, Rx Only, 10 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135,NDC 99999-2011-17

Affected lot / code info
Lot #s: 04102015@38, BUD: 9/1/2015; 03132015@37, BUD: 7/11/2015; 04172015@28, BUD: 10/14/2015

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
113 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-1311-2015. 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