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Class I · Most seriousActive recall

Potassium Chloride

A reasonable chance it could cause serious harm or death.

Does this affect you?
Check your lot numberLot 1023172, Exp Date: 31 January 2026
Where it was soldNationwide 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

Labeling: Label Error on Declared Strength. Overwrap labeled as Potassium Chloride Inj 10 mEq may contain flexible containers of Potassium Chloride Inj 20 mEq

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 byICU Medical Inc.
Brand namePOTASSIUM CHLORIDE
Generic namePOTASSIUM CHLORIDE
Active ingredient(s)POTASSIUM CHLORIDE
Distributed by / forICU Medical, Inc.
NDC0990-7074-26
Show the full FDA record
Full product labelPOTASSIUM CHLORIDE Inj., 10 mEq total in 100 mL, 100 mEq/L flexible container, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7074-26; Bar Code (01)00309907074269
Recalling firmICU Medical, Inc.
DistributionNationwide in the USA
Quantityunknown
Recall initiated2025-02-13
Report date2025-03-19
Recall completed—
Recall numberD-0268-2025
ClassificationClass I
FDA statusOngoing
Origin on fileLake Forest IL United States

Related

Potassium chloride recallsRecent drug recallsCheck another medication

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.