US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 26, 2024 (2 years ago)

Potassium Chloride Micro 10mEq K (750 mg) Extended Release Capsules, 30-count blister…

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

Why it was recalled

CGMP Deviations: Out of specification for dissolution

What was recalled

Potassium Chloride Micro 10mEq K (750 mg) Extended Release Capsules, 30-count blister card, Rx only, MFG: Glenmark, Mahwah, NJ 07430, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC 70518-1203-03

Recalling firm
RemedyRepack Inc.
NDC code
70518-1203-03
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0611-2024

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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