Benzphetamine Hydrochloride Tablets — Class III drug recall D-1057-2016
Terminated recall by KVK-Tech, Inc., reported 2016-07-06, distributed nationwide. Discoloration: presence of scuffing marks on tablets.
| Recall number | D-1057-2016 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | KVK-Tech, Inc., Newtown, PA, United States |
| Recall initiated | 2016-05-05 |
| Classified | 2016-06-28 |
| Reported by FDA | 2016-07-06 |
| Terminated | 2017-01-13 |
| Distributed | Nationwide (US) |
| NDC | 10702-0040-03 |
| Lot numbers | 12825A, 12937A, 8/18 |
Product
Benzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH, INC., Newtown, PA 18940, NDC 10702-0040-03
Reason for recall
Discoloration: presence of scuffing marks on tablets.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1057-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.