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.
Reported: February 25, 2015 Initiated: October 6, 2014 #D-0387-2015
Product Description
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.
Details
- Recalling Firm
- Hospira Inc.
- Units Affected
- 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.
- Location
- Lake Forest, IL
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Hospira Inc.. Units affected: 200 vials.
Why was this product recalled? ▼
Temperature Abuse: Products experienced uncontrolled temperature excursions during transit.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 25, 2015. Severity: Moderate. Recall number: D-0387-2015.
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