FDAFDA · Food and drugs·Recall number D-1148-2014
Heparin Sodium Injection, USP 10,000 USP units per 10 mL (1,000 USP units per mL) For IV or SC use, Multi-Dose Vial, Rx only, NDC 63323-540-11, 25 vials in tray, each boxed vial individually labeled as: Heparin Sodium Injection, USP 10,000 USP units per 10 mL (1,000 USP units per mL) For IV or SC use, Multi-Dose Vial, Rx only, NDC 63323-540-11.
Published March 12, 2014 · Recall initiated: January 22, 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
Subpotent; 18 month time point
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- HEPARIN SODIUM
- Manufacturer
- Fresenius Kabi USA, LLC
- Distributor
- Nationwide
- UPC
- 0363323276010
- Lot
- Lot Number: 6004137, Expiration date: 06/2014
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.