Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to Presence of Particulate Matter: Confirmed customer compliants of...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Baxter Healthcare Corp. directly.
Affected Products
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
Quantity: 255,852 VIAFLEX Plastic Containers
Why Was This Recalled?
Presence of Particulate Matter: Confirmed customer compliants of finding an insect floating in the primary container of each product.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Baxter Healthcare Corp.
Baxter Healthcare Corp. has 126 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report