Reported Dec 3, 2014 · Terminated
0.9% Sodium Chloride Injection, USP, 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045,…
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?
- 0.9% Sodium Chloride Injection, USP, 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-09.
- Lot codes and dates
25 of 25 products
Products covered by this recall # Product as published 1 Lot # 32-044-JT 2 Exp. 08/15 Lot # 32-072-JT 3 Exp. 08/15 Lot # 32-102-JT 4 Exp. 08/15 Lot # 33-028-JT 5 Exp. 09/15 Lot # 33-046-JT 6 Exp. 09/15 Lot # 33-049-JT 7 Exp. 09/15 Lot # 33-061-JT 8 Exp. 09/15 Lot # 33-085-JT 9 Exp. 09/15 Lot # 33-096-JT 10 Exp. 09/15 Lot # 33-101-JT 11 Exp. 09/15 Lot # 33-102-JT 12 Exp. 09/15 Lot # 34-016-JT 13 Exp. 10/15 Lot # 34-085-JT 14 Exp. 10/15 Lot # 34-122-JT 15 Exp. 10/15 Lot # 34-123-JT 16 Exp. 10/15 Lot # 35-026-JT 17 Exp. 11/15 Lot # 35-030-JT 18 Exp. 11/15 Lot # 35-067-JT 19 Exp. 11/15 Lot # 36-002-JT 20 Exp. 12/15 Lot # 36-029-JT - Amount recalled
- 16,487,040 bags
This recall covers 13 products
The agency filed one notice per product. You are reading one of them; the other 12 are below.
Where it was sold
- Nationwide
- PR
Why it was recalled
Lack of Assurance of Sterility: Potential of punctures through the overwrap and primary container which may result in IV bag leaks.
This product could cause temporary or reversible health problems — stop using it.
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