US Drug Recall Register
Class II · Moderate risk Terminated Initiated Nov 10, 2014 (12 years ago)

Potassium Chloride Injection, 10mEq per 100mL, 100 mL Sterile single dose container bags…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Labeling: Label Error On Declared Strength: Bags of Potassium Chloride 10 mEq per 100 mL were incorrectly overpouched with wraps labeled as Potassium Chloride Injection, 20 mEq per 100 mL.

What was recalled

Potassium Chloride Injection, 10mEq per 100mL, 100 mL Sterile single dose container bags, Rx only, Baxter USA, NDC 0338-0709-48, Product Code 2B0826.

Recalling firm
Baxter Healthcare Corp.
NDC code
0338-0709-48
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0256-2015

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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