Potassium Chloride Micro 10mEq K — Class II drug recall D-0611-2024
Terminated recall by RemedyRepack Inc., reported 2024-07-24, distributed nationwide. CGMP Deviations: Out of specification for dissolution
| Recall number | D-0611-2024 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | RemedyRepack Inc., Indiana, PA, United States |
| Recall initiated | 2024-06-26 |
| Classified | 2024-07-18 |
| Reported by FDA | 2024-07-24 |
| Terminated | 2025-01-31 |
| Distributed | Nationwide (US) |
| Quantity | 142 blister |
| Reason classes | cgmp, specification failure |
| NDC | 70518-1203-03 |
| Lot numbers | J0751898-011424, J0758674-021824 |
| Expiration dates | 2025-01-31, 2025-03-31 |
Product
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
Reason for recall
CGMP Deviations: Out of specification for dissolution
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-0611-2024. 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.