Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 0990-7075-26 recalled?

Potassium Chloride · 24 POUCH in 1 CASE (0990-7075-26) / 1 BAG in 1 POUCH / 100 mL in 1 BAG

Yes — this exact package was recalled

1 FDA recall names the code 0990-7075-26 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

1 of these recalls is still ongoing.

Active ingredient
Potassium Chloride
Strength
POTASSIUM CHLORIDE 200 meq/1000mL
Form
Injection, Solution · Intravenous
Labeler
ICU Medical Inc.
Type
Human Prescription Drug
Product code
0990-7075

Recalls naming this package

Class I ยท High risk

POTASSIUM CHLORIDE Inj.

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.

Ongoing Labeling / mix-up ICU Medical, Inc. NDC 0990-7075-26 D-0267-2025

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler