Drug product
Sodium Thiosulfate 25%, 250 mg/mL (12.5 g/50mL), PF Sterile Solution for Injection, 50 mL Single Dose Vial, For Office Use Only, JCB Laboratories, Wichita, KS.
D-1044-2013
Product summary
- Firm
- JCB Labs LLC
- Event
- Event 66099
- Status
- Terminated
- Classification
- Class II
- Quantity
- 1056 vials
- Official record key
drug-enforcement:D-1044-2013
Official wording
Reason: Lack of Assurance of Sterility: The product lots are being recalled due to laboratory results (from a contract lab) indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable. Hence the sterility of the products cannot be assured.
Code information: Lot #: 130701@9, Exp 12/28/2013; 130709@6, Exp 01/05/2014; 130717@2, Exp 01/13/2014
Distribution pattern: Nationwide and Guam
Derived failure modes
-
Microbial contamination
microbial contamination
-
Sterility assurance
Lack of Assurance of Sterility