FDA Drug recall D-0850-2026
Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL, 60016, Made in USA, NDC 00338-0719-06
- FDA Drug
- Class I
- ongoing
- Published 2026-09-16
On 2026-09-16 the FDA classified a Class I recall of Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL, 60016, Made in USA, NDC 00338-0719-06 by Baxter Healthcare, citing presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0850-2026 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2026-08-17 |
| Published | 2026-09-16 |
| Last updated | 2026-09-23 05:30 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
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.
Identifiers
| code_info | Lot #: Y495066, Exp. Date July 31, 2027 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-23 05:30 UTC. Current status: ongoing.
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Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0850-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.