Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only,… was recalled on August 17, 2026 in cooperation with the U.S. Food and Drug Administration because presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution..
Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL, 60016, Made in USA, NDC 00338-0719-06
Lot #: Y495066, Exp. Date July 31, 2027
Units affected: 606 bags
Where it was sold: U.S. Nationwide.
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: particulate matter identified as stainless steel particles in the solution.
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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