ICU Medical Inc recalls 0.9% Sodium Chloride Injection, USP in 1000 mL Single Dose Flexible Container, Hospira, Inc., Lake Forest, IL 60045 USA…
- Recall date
- July 26, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-1091-2017
- FDA classification
- Class II
- Brand / firm
- ICU Medical Inc
- Sold / distributed
- Nationwide
Why it was recalled
Presence of Particulate Matter; stainless steel
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 in 1000 mL Single Dose Flexible Container, Hospira, Inc., Lake Forest, IL 60045 USA --- NDC# 0409-7983-09
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