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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 #: J6B435, J6B444, J6B457, Exp Date: 30APR2027.
Where it was soldNationwide within the United States
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: particulate matter identified as iron oxide, inorganic material, cellulose cotton fiber or polystyrene

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 byB. Braun Medical Inc.
Brand nameSODIUM CHLORIDE
Generic nameSODIUM CHLORIDE
Active ingredient(s)SODIUM CHLORIDE
Distributed by / forB BRAUN MEDICAL INC
NDC0264-1800-32
Show the full FDA record
Full product label0.9% Sodium Chloride Injection, USP, 100 mL Partial Fill in 150 mL PAB Container, Sterile, Rx only, B. Braun Medical Inc., Bethlehem, PA 18018 USA, NDC 0264-1800-32.
Recalling firmB BRAUN MEDICAL INC
DistributionNationwide within the United States
Quantity201,472 total container
Recall initiated2026-08-19
Report date2026-09-16
Recall completed—
Recall numberD-0869-2026
ClassificationClass I
FDA statusOngoing
Origin on fileAllentown PA 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.