Baxter Healthcare Corporation recalls Dextrose Injection
- Recalling company
- Baxter Healthcare Corporation
- Product
- Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL, 60016, Made in USA, NDC 00338-0719-06
- Reason
- Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution.
- Classification
- Class I – a reasonable probability that use will cause serious adverse health consequences or death
- Recall date
- Aug 17, 2026
- Reported
- Sep 16, 2026
- Distribution
- U.S. Nationwide.
- Status
- Ongoing
- Quantity
- 606 bags
- Lot / codes
- Lot #: Y495066, Exp. Date July 31, 2027
- Company location
- Deerfield, IL
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0850-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0850-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.