Data Foundry

Drug recalls 2024

Potassium Chloride Extended-Release Capsules — Class II drug recall D-0606-2024

Ongoing recall by Glenmark Pharmaceuticals Inc., USA, reported 2024-07-24, distributed nationwide. CGMP Deviations

Recall numberD-0606-2024
Product typeDrug
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmGlenmark Pharmaceuticals Inc., USA, Mahwah, NJ, United States
Recall initiated2024-05-30
Classified2024-07-17
Reported by FDA2024-07-24
DistributedNationwide (US)
Reason classescgmp
NDC68462-0357, 68462-0357-01, 68462-0357-05, 68462-0357-90
Lot numbers17230074, 17230221, 17230468, 17230479, 17230543, 17230553, 17230561, 17230619, 17230624, 17230879, 17230890, 17230918, 17230984, 17230996, 17231002, 17231081, 17231102, 17231135, 17231329, 17231369, 17231513, 17231516, 17231713, 17231903, 17231909, 17231943, 17232166, 17232179, APR-30-25, AUG-31-25, DEC-31-24, FEB-28-25, JAN-31-25, JUL-31-25, JUN-30-25, MAR-31-25, MAY-31-24, SEP-30-25

Product

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

Reason for recall

CGMP Deviations

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0606-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.