Heparin Sodium in 5% Dextrose Injection, Heparin, 25,000 USP Heparin Units/250 mL (100 USP Heparin Units/mL), 250 mL, Single-Dose Container, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7793-62
Reported: July 16, 2014 Initiated: June 6, 2014 #D-1425-2014
Product Description
Heparin Sodium in 5% Dextrose Injection, Heparin, 25,000 USP Heparin Units/250 mL (100 USP Heparin Units/mL), 250 mL, Single-Dose Container, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7793-62
Reason for Recall
Lack of Assurance of Sterility: Confirmed consumer report of fluid leaking from primary container of bag.
Details
- Recalling Firm
- Hospira Inc.
- Units Affected
- 142,152 bags
- Distribution
- Nationwide
- Location
- Lake Forest, IL
Frequently Asked Questions
What product was recalled? ▼
Heparin Sodium in 5% Dextrose Injection, Heparin, 25,000 USP Heparin Units/250 mL (100 USP Heparin Units/mL), 250 mL, Single-Dose Container, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7793-62. Recalled by Hospira Inc.. Units affected: 142,152 bags.
Why was this product recalled? ▼
Lack of Assurance of Sterility: Confirmed consumer report of fluid leaking from primary container of bag.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 16, 2014. Severity: Moderate. Recall number: D-1425-2014.
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