Class II · ModerateRecall completed
Potassium Chloride Micro 10mEq K (750 mg) Extended Release Capsules
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberLot #: J0758674-021824, Exp 03/31/2025; J0751898-011424, Exp 01/31/2025
Where it was soldUSA Nationwide
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
CGMP Deviations: Out of specification for dissolution
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
| Distributed by / for | RemedyRepack Inc. |
| NDC | 70518-1203-03 |
Show the full FDA record
| Full product label | 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 |
| Recalling firm | RemedyRepack Inc. |
| Distribution | USA Nationwide |
| Quantity | 142 blister cards, 30 per blister card |
| Recall initiated | 2024-06-26 |
| Report date | 2024-07-24 |
| Recall completed | 2025-01-31 |
| Recall number | D-0611-2024 |
| Classification | Class II |
| FDA status | Terminated |
| Origin on file | Indiana PA United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.