FDA recall D-0849-2026

Product

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

Reason for recall

Presence of particulate matter: Particulates identified as fiberglass

Distribution

Natonwide in the USA

Key facts

Status

Ongoing

Initiation date

2026-08-17

Report date

2026-09-09

Voluntary/Mandated

Voluntary: Firm initiated

Location

Deerfield, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0849-2026