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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…

Presence of particulate matter: Particulates identified as fiberglass

Class I Medicine & devices FDA September 9, 2026
Read the official FDA notice →

What to do

Stop using the product and check it against the description above. This recall is in the most serious category, meaning the agency believes it can cause serious injury or death — don't finish the package or use up what's left. If you or a family member has already been affected, keep the packaging and the lot code — they're what a claim rests on later.

Details

Recalling company
Baxter Healthcare Corporation — Deerfield, IL
Severity
Class I — serious
Reported
September 9, 2026
Quantity
145,464 500mL bags
Recall number
D-0849-2026
Status
Ongoing
Source
FDA

Where it went

Natonwide in the USA

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