Drug recall D-0387-2015
Product
Vancomycin Hydrochloride for Injection, USP, 500 mg Sterile Powder per Fliptop Vial, packaged in 10 Units per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4332-01.
Reason for recall
Temperature Abuse: Products experienced uncontrolled temperature excursions during transit.
Lots and codes
One shipment of Lot #: 34-366-8E02; Exp 1OCT2015 to The Harvard Drug Group, Livonia, MI
Recall details
- Recalling firm
- Hospira Inc., Lake Forest, IL
- Quantity
- 200 vials
- Distribution
- Distribution limited to one shipment to The Harvard Drug Group, Livonia, MI for the lots of Vancomycin 500 mg, Ketorolac tromethamine 60 mg/2 mL (30 mg/mL), and Propofol 1% 200 mg/20 mL (10 mg/mL), these lots remained within the control of the distributor and were not further distributed. Distribution was Nationwide for the Vancomycin 1 g product.
- Type
- Voluntary: Firm initiated
- Recall initiated
- October 6, 2014
- Terminated
- December 15, 2016
Related products
- Vancomycin Hydrochloride – drug information
- NDC 0409-4332 Vancomycin Hydrochloride · Vancomycin Hydrochloride 500 mg/1 · Hospira, Inc.
- NDC 0409-6531 Vancomycin Hydrochloride · Vancomycin Hydrochloride 750 mg/1 · Hospira, Inc.
- NDC 0409-3515 Vancomycin Hydrochloride · Vancomycin Hydrochloride 1.5 g/1 · Hospira, Inc.
- NDC 0409-6533 Vancomycin Hydrochloride · Vancomycin Hydrochloride 1 g/1 · Hospira, Inc.