FDAFDA · Food and drugs·Recall number D-1595-2014
COUMADIN FOR INJECTION (Warfarin Sodium for Injection, USP 5 mg Single-Use Vial Rx Only Distributed by Bristol Meyers Squibb Company, Princeton, NJ 08543 USA NDC 0590-0324-96
Published September 24, 2014 · Recall initiated: May 12, 2014
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
Presence of Particulate Matter: particulate matter identified as metallic-like and non-metallic cellulose fiber particles found in retain vials
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Bristol-Meyers Squibb
- Distributor
- Nationwide, Canada
- Lot
- Lot 00201125, Exp. 09/14; 00201126 Exp.11/14; 00201127, Exp.12/14; 00201228 Exp.06/15; 00201229 Exp. 07/15; 00201230, Exp. 09/15
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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