0.9% Sodium Chloride Injection USP 500 mL, VIAFLEX Plastic… was recalled on August 17, 2026 in cooperation with the U.S. Food and Drug Administration because presence of particulate matter: Particulates identified as fiberglass.
0.9% Sodium Chloride Injection USP 500 mL, VIAFLEX Plastic Containers, with 24 units per case. Baxter Healthcare Corporation, Deerfield, IL, 60015, USA, Made in USA, NDC 0338-0049-03
Lot: Y495523, Y495523A, Exp 31-Oct-2027
Units affected: 145,464 500mL bags
Where it was sold: Natonwide in the USA
Compare the codes above against the label on your product — usually on the bottom, the back panel, or the packaging. If your unit isn't listed, it is not part of this recall.
Presence of particulate matter: Particulates identified as fiberglass
Class I is the most serious FDA recall level: using or being exposed to the product could cause serious health problems or death.
Stop using the product. Return it to the place of purchase for a refund, or dispose of it. Contact the recalling firm with questions.
Contact: Recalling firm: Baxter Healthcare Corporation
Not sure what you're entitled to? Read our guide: what to do if your product is recalled.
Always confirm details on the official notice from the U.S. Food and Drug Administration before acting.
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