# FDA recall D-0611-2024

> **RemedyRepack Inc.** · Class II · drug recall initiated 2024-06-26.

## 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

## Distribution

USA Nationwide

## Key facts

- **Recall number:** D-0611-2024
- **Recalling firm:** RemedyRepack Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2024-06-26
- **Report date:** 2024-07-24
- **Termination date:** 2025-01-31

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Indiana, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0611-2024

## Citation

> AI Analytics. FDA recall D-0611-2024. Retrieved 2026-06-14 from https://api.ai-analytics.org/recall/D-0611-2024. Source: US FDA. Licensed CC0.

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