FDA Drug · D-0849-2026

0.9% Sodium Chloride Injection USP 500 mL, VIAFLEX Plastic Containers, with 24 units per case. Baxter Healthcare Corporation, Deerfield, IL, 60015, USA, Made in USA, NDC 0338-0049-03

Class I · Ongoing

Presence of particulate matter: Particulates identified as fiberglass

Affected lots / codes — check yours against thisLot: Y495523, Y495523A, Exp 31-Oct-2027

Recalling firm: Baxter Healthcare Corporation, Deerfield, IL
Classification: Class I (most serious — risk of serious harm)
Status: Ongoing
Quantity: 145,464 500mL bags
Distribution: Natonwide in the USA
Recall initiated: August 17, 2026
Classified: September 15, 2026
Initiation: Voluntary: Firm initiated

Official source. This record is published by the U.S. FDA through the openFDA enforcement database. View the unmodified government record:
https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0849-2026%22

Important. Recalls target specific lots and codes — compare the affected lots above against your own product. This page reproduces public FDA data for readability; EveryRecall is independent and not affiliated with the FDA.

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