ICU Medical recalls 20 mEq potassium chloride injections due to label error. Cases may contain containers mislabeled as 10 mEq instead of 20 mEq. Correct dosage is printed on the flexible container.
Labeling: Label Error on Declared Strength. Cases labeled POTASSIUM CHLORIDE 20 mEq, may contain flexible containers with overwrap mislabeled as 10 mEq. The correct dosage strength of 20 mEq is printed on the labeling affixed to the product flexible container.
ICU Medical is recalling potassium chloride injections that may have a label error. The product could be mislabeled as 10 mEq instead of 20 mEq, which could lead to incorrect dosing if used without checking the label.
The product may have a label error where flexible containers are mislabeled as 10 mEq instead of 20 mEq. This could lead to incorrect dosing if the healthcare provider uses the product without verifying the label. The correct dosage strength is printed on the flexible container itself.
Healthcare professionals using these injections for medical purposes. Patients receiving treatment with the recalled product may be at risk if the label error causes incorrect dosing.
Check for the product name 'Potassium Chloride Injections', 20 mEq total in 100 mL, 24 x case. Look for the lot number 1023172 and expiration date of January 31, 2026.
Verify the dosage strength printed on the flexible container itself, which should be 20 mEq.
No, the product is safe if the label is checked correctly. The correct dosage strength is printed on the flexible container.
Look for the product name 'Potassium Chloride Injections', 20 mEq total in 100 mL, 24 x case with lot number 1023172 and expiration date of January 31, 2026.
No, you can continue using it as long as you check the label on the flexible container for the correct dosage strength of 20 mEq.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall D-0267-2025 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall D-0267-2025 from ICU Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
