FDA Drugs recall ·
Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only… recall
This is an FDA Class I recall — the most serious type.
- Recall number
- D-0850-2026
- Date
- (initiated August 17, 2026)
- Company / brand
- Baxter Healthcare Corporation
1 Baxter Pkwy, Deerfield, IL, United States - Category
- Drugs › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- 606 bags
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL, 60016, Made in USA, NDC 00338-0719-06
Why was it recalled?
Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot #: Y495066, Exp. Date July 31, 2027
Distribution
U.S. Nationwide.
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (drugs), recall D-0850-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.