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Class I · Most seriousActive recall

Sodium Chloride

A reasonable chance it could cause serious harm or death.

Does this affect you?
Check your lot numberLot: Y495523, Y495523A, Exp 31-Oct-2027
Where it was soldNatonwide in the USA
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Presence of particulate matter: Particulates identified as fiberglass

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byMade in USA
Brand nameSODIUM CHLORIDE
Generic nameSODIUM CHLORIDE
Active ingredient(s)SODIUM CHLORIDE
Distributed by / forBaxter Healthcare Corporation
NDC0338-0049-03
Show the full FDA record
Full product label0.9% 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 firmBaxter Healthcare Corporation
DistributionNatonwide in the USA
Quantity145,464 500mL bags
Recall initiated2026-08-17
Report date2026-09-09
Recall completed
Recall numberD-0849-2026
ClassificationClass I
FDA statusOngoing
Origin on fileDeerfield IL United States

Related

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.