Reported Jul 16, 2014 · Terminated
Heparin Sodium in 5% Dextrose Injection, Heparin, 25,000 USP Heparin Units/250 mL (100 USP Heparin Units/mL), 250 mL,…
Hospira Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Hospira Inc. · 275 N Field Dr · Lake Forest, IL · 60045-2579
Is this the product you have?
- 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
- Lot codes and dates
Lot # 34-811-KL36-106-KL36-114-KLExp. 12/1536-101-KLExp. 12/1537-202-KLExp. 1/1638-302-KLExp. 2/1638-305-KLExp. 2/16
- Amount recalled
- 142,152 bags
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
- Nationwide
Why it was recalled
Lack of Assurance of Sterility: Confirmed consumer report of fluid leaking from primary container of bag.
This product could cause temporary or reversible health problems — stop using it.
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