FDA Media Alert Detail

Drug Recall

FDA Drug Recall: Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL, 6...

  • U.S. Food and Drug Administration
  • September 16, 2026
  • ID: D-0850-2026

Drug Enforcement Report Details

Recall NumberD-0850-2026
Recalling FirmBaxter Healthcare Corporation
ClassificationClass I
Voluntary / MandatedVoluntary: Firm initiated
Distribution PatternU.S. Nationwide.
StatusOngoing
Product Description

Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL, 60016, Made in USA, NDC 00338-0719-06

Reason for Recall

Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution.

Code Information

Lot #: Y495066, Exp. Date July 31, 2027


Content syndicated from the U.S. Food and Drug Administration (FDA) drug enforcement reports database.