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Class IOngoing

Baxter Healthcare Corporation recalls 0

Recall date · record updated Sep 9, 2026 · Source: U.S. Food and Drug Administration (openFDA drug enforcement)

What to do

Check your product against the names and codes above. The FDA enforcement record lists the recall as voluntary: firm initiated; it does not state a consumer remedy, so follow the firm’s notice or the FDA link.

Company
Baxter Healthcare Corporation
Reason
Presence of particulate matter: Particulates identified as fiberglass
Hazard
FDA Class I: a reasonable probability that use or exposure will cause serious adverse health consequences or death (FDA definition).
Who’s affected
Natonwide in the USA
Official notice
www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99678…

Products

  1. 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

    Codes/lots: Lot: Y495523, Y495523A, Exp 31-Oct-2027Quantity: 145,464 500mL bagsRecall no. D-0849-2026Class I

Update history

  1. First listed on OVERLOOKED from the official record.

When the agency expands or changes this recall, we update this page and log the change here.

Proof: raw official record (JSON) · fetched from FDA API

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