D-1139-2015 Class III Terminated
Recall Details
- Product Type
- Drugs
- Report Date
- June 24, 2015
- Initiation Date
- May 13, 2015
- Termination Date
- April 6, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 14,649 Cartons
Product Description
Fentanyl Citrate Inj., USP, CII, 250 mcg/5 mL (50 mcg/mL) (0.05 mg/mL), Rx Only, For IV or IM Use Preservative Free, 25 X 5 mL Single Dose Vials per Carton, Manufactured by: West-Ward, Eatontown, NJ 07724 USA, NDC 0641-6028-25.
Reason for Recall
Failed Impurities/Degradation Specifications; 12 month stability testing (Expansion of RES #70548).
Distribution Pattern
Nationwide
Code Information
Lot #: 043410, Exp 04/2015; 053391, Exp 05/2015; 073340, Exp 07/2015; 083330, 083333, 083335, Exp 08/2015; 093319, 093321, 093323, Exp 09/2015; 103316, 103318, Exp 10/2015