Class I recall: Baxter Healthcare Corporation: 0.9% Sodium Chloride Injection USP 500 mL, VIAFLEX Plastic Containers, with 24 u

Baxter Healthcare Corporation has issued a Class I recall for 0.9% Sodium Chloride Injection USP, 500 mL, in VIAFLEX plastic containers, NDC 0338-0049-03. The recall states the product may contain particulate matter identified as fiberglass. FDA classifies this as a Class I recall, indicating the most serious recall category.

Most relevant for: Clinical settings that stock or administer this specific lot of Baxter 0.9% Sodium Chloride Injection USP in 500 mL VIAFLEX containers for intravenous use.

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