CLASS II ONGOING Drug recall · Reported 24 Jul 2024 · FDA Enforcement Report

Potassium Chloride Extended-Release Capsules, USP, (750 mg) 10 mEq K recalled

Glenmark Pharmaceuticals Inc., U is recalling Potassium Chloride Extended-Release Capsules, USP, (750 mg) 10 mEq K, distributed nationwide in the US. The recall was initiated on 30 May 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 17230074, 17230221, Exp Dec-31-24; 17230468, 17230479, 17230553, 17230543, 17230561, Exp Jan-31-25; 17230619, 17230624, Exp Feb-28-25; 17230879, 17230890, 17230918, 17230984, 17230996, 17231002, 17231081, Exp Mar-31-25; 17231102, 17231135, 17231329, Exp Apr-30-25; 17231369, 17231513, Exp May-31-24; 17231516, 17231713, Exp Jun-30-25; 17231909, 17231903, Exp Jul-31-25; 17231943, Exp Aug-31-25; 17232166, 17232179, Exp Sep-30-25.
NDC68462-357

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0606-2024
FDA event ID
94715
Recalling firm
Glenmark Pharmaceuticals Inc., U, Mahwah, NJ
Manufacturer
Glenmark Pharmaceuticals Inc., USA
Classification
Class II
Status
Ongoing
Recall initiated
30 May 2024
FDA classified
17 Jul 2024
Reported
24 Jul 2024
Type
Voluntary: Firm initiated
Customers notified by
Letter

Timeline

30 May 2024Recall initiated by company
17 Jul 2024Classified by FDA+48 days
24 Jul 2024Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

CGMP Deviations

Product as listed by the FDA

Potassium Chloride Extended-Release Capsules, USP, (750 mg) 10 mEq K, 100-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 68462-357-01

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Is Potassium Chloride Extended-Release Capsules, USP, (750 mg) 10 mEq K recalled?

Yes. Glenmark Pharmaceuticals Inc., U recalled Potassium Chloride Extended-Release Capsules, USP, (750 mg) 10 mEq K on 30 May 2024. The recall is Class II and its status is Ongoing. Recall number D-0606-2024.

Why was it recalled?

CGMP Deviations

Which lots are affected?

Lot #: 17230074, 17230221, Exp Dec-31-24; 17230468, 17230479, 17230553, 17230543, 17230561, Exp Jan-31-25; 17230619, 17230624, Exp Feb-28-25; 17230879, 17230890, 17230918, 17230984, 17230996, 17231002, 17231081, Exp Mar-31-25; 17231102, 17231135, 17231329, Exp Apr-30-25; 17231369, 17231513, Exp May-31-24; 17231516, 17231713, Exp Jun-30-25; 17231909, 17231903, Exp Jul-31-25; 17231943, Exp Aug-31-25; 17232166, 17232179, Exp Sep-30-25.

Where was it sold?

Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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