Class I ยท High risk
POTASSIUM CHLORIDE Inj.
Labeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj. 10 mEq instead of POTASSIUM CHLORIDE Inj. 20 mEq
National Drug Code
Is NDC 0990-7077-14 recalled?
Potassium Chloride · 24 POUCH in 1 CASE (0990-7077-14) / 1 BAG in 1 POUCH / 50 mL in 1 BAG
Yes — this exact package was recalled
1 FDA recall names the code 0990-7077-14 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 400 meq/1000mL
- Form
- Injection, Solution · Intravenous
- Labeler
- ICU Medical Inc.
- Type
- Human Prescription Drug
- Product code
- 0990-7077
Recalls naming this package
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
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