FDAFDA · Food and drugs·Recall number D-1023-2018
Daptomycin for Injection, 500 mg per vial, packaged as 1 Single-dose vial per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-0106-01.
Published August 8, 2018 · Recall initiated: June 28, 2018
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Microbial Contamination of Sterile Products: Product associated with reports of adverse events indicative of infusion reactions related to microbiological contamination.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- PFIZER
- Distributor
- Nationwide in the USA and Puerto Rico.
- Lot
- Lot #: 712453A, Exp 1-Nov-18; 771803A, Exp 1-May-19; 792103A, Exp 1-Jul-19; 800903A, Exp 1-Aug-19; 810853A, Exp 1-Sep-19; 841703A, 841753A, Exp 1-Dec-19; 850553A, Exp 1-Jan-20.
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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