Baxter Healthcare Corporation recalls 0.9% Sodium Chloride Injection USP 500 mL
- Recalling company
- Baxter Healthcare Corporation
- 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
- Presence of particulate matter: Particulates identified as fiberglass
- Classification
- Class I – a reasonable probability that use will cause serious adverse health consequences or death
- Recall date
- Aug 17, 2026
- Reported
- Sep 9, 2026
- Distribution
- Natonwide in the USA
- Status
- Ongoing
- Quantity
- 145,464 500mL bags
- Lot / codes
- Lot: Y495523, Y495523A, Exp 31-Oct-2027
- Company location
- Deerfield, IL
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0849-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0849-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.