Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Benzphetamine Hydrochloride Tablets Recalled by KVK-Tech, Inc. Due to Discoloration: presence of scuffing marks on tablets.
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
Benzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH, INC., Newtown, PA 18940, NDC 10702-0040-03
Quantity: 9360 bottles of lot # 12825A and 7284 bottles of lot # 12937A
Why Was This Recalled?
Discoloration: presence of scuffing marks on tablets.
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