Hospira Inc. recalls 0.9% Sodium Chloride Injection, USP, 100 mL ADD-Vantage Unit, Rx only, Manufactured by Hospira Inc., Lake Forest, IL, 6…
- Recall date
- April 7, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0490-2015
- FDA classification
- Class II
- Brand / firm
- Hospira Inc.
- Sold / distributed
- Nationwide
Why it was recalled
Lack of Sterility Assurance: The product has the potential 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, 100 mL ADD-Vantage Unit, Rx only, Manufactured by Hospira Inc., Lake Forest, IL, 60045, NDC: 0409-7101-67
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