FDA Drug Recalls

Recalls / Class II

Class IID-1304-2015

Product

SIU-Tri-Mix 6/0.33/3.33 Injection Solution, Rx Only, 3 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 13429-2007-70

Affected lot / code info
Lot #: 03192015@27, BUD 07/13/2015

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
2.5 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-1304-2015. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.