Baxter Healthcare Corp. recalls 0.9% Sodium Chloride Injection, USP, 250 mL VIAFLEX Plastic Container Bag, Rx Only, Manufactured by Baxter Healthcare C…
- Recall date
- December 15, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0957-2016
- FDA classification
- Class I
- Brand / firm
- Baxter Healthcare Corp.
- Sold / distributed
- Nationwide
Why it was recalled
Presence of Particulate Matter: Confirmed customer compliants of finding an insect floating in the primary container of each product.
Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.
What was recalled
0.9% Sodium Chloride Injection, USP, 250 mL VIAFLEX Plastic Container Bag, Rx Only, Manufactured by Baxter Healthcare Corporation, Deerfield, IL 60015, NDC 0338-0049-02
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