Baxter Healthcare Corporation recalls 0.9% Sodium Chloride Injection USP 500 mL, VIAFLEX Plastic C
See all recalls from Baxter Healthcare Corporation →Recalled 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
Hazard / Issue
Presence of particulate matter: Particulates identified as fiberglass
Issued by
FDA
Distribution: Natonwide in the USA
Lot/Code Info: Lot: Y495523, Y495523A, Exp 31-Oct-2027
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
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Search Amazon for 0.9% Sodium Chloride Injection →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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