Reported Jul 3, 2013 · Terminated
20% Dextrose Injection, USP, a) 500 mL in 1000 mL Partial-Fill Container (NDC 0409-7935-19), b) 500 mL VisIV Container…
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?
3 of 3 products
| # | Product as published |
|---|---|
| 1 | 500 mL in 1000 mL Partial-Fill Container (NDC 0409-7935-19) |
| 2 | 500 mL VisIV Container (NDC 0409-7953-30) |
| 3 | 1000 mL VisIV Container, (NDC 0409-7953-48), Rx Only, Hospira, Inc., Lake Forest, IL 60045 |
- Lot codes and dates
Lot #: a) 09-183-JTExp 3/13b) 01-081-JTExp 7/12c) 07-078-JT91-083-JTExp 7/12
- Amount recalled
- 216,396 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.
Want the full recall guide?
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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