US Drug Recall Register
Class III · Low risk Terminated Initiated May 5, 2016 (10 years ago)

Benzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Discoloration: presence of scuffing marks on tablets.

What was recalled

Benzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH, INC., Newtown, PA 18940, NDC 10702-0040-03

Recalling firm
KVK-Tech, Inc.
NDC code
10702-0040-03
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1057-2016

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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