Hospira product recalled over sterility concerns
- Recall date
- December 22, 2014
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Hospira Inc. recalls 0.9% Sodium Chloride Injection, USP, 100mL, VisIV Container, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-798…
- Recall number
- D-0334-2015
- FDA classification
- Class II
- Brand / firm
- Hospira Inc.
- Sold / distributed
- Nationwide
Why it was recalled
Lack of Assurance of Sterility: The product has the potential for solution to leak at the administrative port.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
0.9% Sodium Chloride Injection, USP, 100mL, VisIV Container, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-7984-11
Get recall alerts
Free email alert whenever Hospira Inc. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Hospira Inc.