Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Indomethacin Extended-Release Capsules USP Recalled by KVK Tech, Inc. Due to cGMP deviations
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact KVK Tech, Inc. directly.
Affected Products
Indomethacin Extended-Release Capsules USP, 75 mg, 100-count bottle, Rx only, Mfd. By: KVK-Tech, Inc., Newtown, PA, 18940, Made in USA, NDC 10702-016-01.
Quantity: 9107 bottles
Why Was This Recalled?
cGMP deviations
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About KVK Tech, Inc.
KVK Tech, Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report