US Drug Recall Register
Class I · High risk Ongoing Initiated May 30, 2024 (2 years ago)

Potassium Chloride Extended-Release Capsules, USP, (750 mg) 10 mEq K, 500-count bottle…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Failed Dissolution Specifications

What was recalled

Potassium Chloride Extended-Release Capsules, USP, (750 mg) 10 mEq K, 500-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd. Plot No. 2, Phase-2, Pharma Zone SEZ, Pithampur, Dist.-Dhar, Madhya Pradesh 454 775, India, Manufactured for: Glenmark Pharmaceuticals Inc, USA, Mahwah, NJ 07430. NDC 68462-357-05

Recalling firm
Glenmark Pharmaceuticals Inc., USA
NDC code
68462-357-05
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0605-2024

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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