Reported Jul 3, 2013 · Terminated
0.9% Sodium Chloride Injection, USP, Polyolefin Flexible Container, a) 500 mL (NDC 0409-7983-30), b) 1000 mL (NDC…
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?
4 of 4 products
| # | Product as published |
|---|---|
| 1 | 500 mL (NDC 0409-7983-30) |
| 2 | 1000 mL (NDC 0409-7983-48) |
| 3 | 250 mL (NDC 0409-7983-02) |
| 4 | 150 mL (NDC 0409-7983-61), Rx Only, by Hospira, Inc., Lake Forest, IL 60045 |
- Lot codes and dates
Lot #: a) 89-135-JT04-224-JT07-138-JTExp 4/1308-160-JT Exp. 8/13b) 08-163-JT90-036-JT02-048-JTExp 2/13c) 93-102-JT11-063-JTExp 9/12d) 93-096-JTExp 11/12
- Amount recalled
- 2,137,660 units
This recall covers 9 products
The agency filed one notice per product. You are reading one of them; the other 8 are below.
Where it was sold
- Nationwide
- PR
Why it was recalled
Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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