Drug recall D-1148-2014
Product
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.
Reason for recall
Subpotent; 18 month time point
Lots and codes
Lot Number: 6004137, Expiration date: 06/2014
Recall details
- Recalling firm
- Fresenius Kabi USA, LLC, Grand Island, NY
- Quantity
- 161,650 vials
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- January 22, 2014
- Terminated
- May 24, 2016
Related products
- Heparin Sodium – drug information
- NDC 63323-276 Heparin Sodium · Heparin Sodium 1000 [USP'U]/mL · Fresenius Kabi USA, LLC
- NDC 63323-543 Heparin Sodium · Heparin Sodium 5000 [USP'U]/.5mL · Fresenius Kabi USA, LLC
- NDC 63323-542 Heparin Sodium · Heparin Sodium 10000 [USP'U]/mL · Fresenius Kabi USA, LLC
- NDC 63323-262 Heparin Sodium · Heparin Sodium 5000 [USP'U]/mL · Fresenius Kabi USA, LLC
- NDC 63323-540 Heparin Sodium · Heparin Sodium 1000 [USP'U]/mL · Fresenius Kabi USA, LLC
- NDC 63323-915 Heparin Sodium · Heparin Sodium 20000 [USP'U]/mL · Fresenius Kabi USA, LLC
- NDC 63323-459 Heparin Sodium · Heparin Sodium 10000 [USP'U]/mL · Fresenius Kabi USA, LLC
- NDC 63323-047 Heparin Sodium · Heparin Sodium 5000 [USP'U]/mL · Fresenius Kabi USA, LLC