Potassium Chloride Micro 10mEq K (750 mg) Extended Release Capsules, 30-count blister card, Rx only, MFG: Glenmark, Mahw
Summary
The FDA issued a Class II for Potassium Chloride Micro 10mEq K (750 mg) Extended Release Capsules, 30-count bl by RemedyRepack Inc.. Reason: CGMP Deviations: Out of specification for dissolution.
Details
Source
Drug Recall
External ID
D-0611-2024
Action Date
2024-07-24
Status
Terminated
Category
drug
Product Description
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
Lot/Code Info: Lot #: J0758674-021824, Exp 03/31/2025; J0751898-011424, Exp 01/31/2025
Quantity Affected: 142 blister cards, 30 per blister card
Reason for Recall
CGMP Deviations: Out of specification for dissolution
Distribution
USA Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2024-06-26
Company
Indiana, PA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 41 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
RemedyRepack Inc. has 34 FDA actions in our database, including 34 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (RemedyRepack Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does RemedyRepack Inc. have FDA actions?
RemedyRepack Inc. has 34 FDA actions in our database, including 34 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0611-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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