FDAFDA · Food and drugs·Recall number D-0095-2019
Meropenem for Injection, USA (I.V.), 1 gram/vial, 25 vials per carton, Sterile, Rx Only, Manufactured for: Hospira, Inc., Lake Forest, IL 60045, USA. NDC carton: 0409-3506-01; NDC vial: 0409-3506-11
Published October 31, 2018 · Recall initiated: September 20, 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
Lack of assurance of sterility: loss of container integrity.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Pfizer Inc.
- Distributor
- Nationwide in the US and Puerto Rico
- Lot
- Lot: 609G047, EXP 10/2018
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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