Class I

Drug Recall: 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

Baxter Healthcare Corporation · August 17, 2026

Reason for Recall

Presence of particulate matter: Particulates identified as fiberglass

Distribution

Natonwide in the USA

States Affected

IN

Quantity Affected

145,464 500mL bags

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0849-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Baxter Healthcare Corporation Drug Recall: 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 | SafeCheck