United States0.9% Sodium Chloride Injection USP 500 mL in VIAFLEX plastic containers (NDC 0338-0049-03), sold in 24‑unit cases and distributed nationwide in the United States, lot numbers Y495523 and Y495523A with expiration 31‑Oct‑2027, is being recalled. The recall is due to presence of particulate matter identified as fiberglass. Owners should check product labels for the above NDC, lot numbers, container type and expiration to see if they have the affected units.
What's being recalled
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
Recalling firm: Baxter Healthcare Corporation, Deerfield, IL, United States.
How to identify it
Lot: Y495523, Y495523A, Exp 31-Oct-2027
The hazard
Presence of particulate matter: Particulates identified as fiberglass
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
Natonwide in the USA
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)