Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Phentermine Hydrochloride Capsules Recalled by KVK-Tech, Inc. Due to Failed Impurities/Degradation Specifications: out-of-specification results for individual unknown...
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
Phentermine Hydrochloride Capsules, USP, 15 mg, packaged in a) 100-count bottle (NDC 10702-0026-01; UPC 3 10702 02601 8) and b) 1000-count bottle (NDC 10702-0026-10; UPC 3 10702 02601 0); Rx only, Mfd. by KVK-TECH, Inc., Newtown, PA
Quantity: 9,696 bottles (100-count), 972 bottles (1000-count)
Why Was This Recalled?
Failed Impurities/Degradation Specifications: out-of-specification results for individual unknown and total impurity at the 12th month room temperature stability test station
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About KVK-Tech, Inc.
KVK-Tech, Inc. has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report