FDA Drug recall D-1057-2016
Benzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH, INC., Newtown, PA 18940, NDC 10702-0040-03
- FDA Drug
- Class III
- terminated
- Published 2016-07-06
On 2016-07-06 the FDA classified a Class III recall of Benzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH, INC., Newtown, PA 18940, NDC 10702-0040-03 by Kvk Tech, citing discoloration: presence of scuffing marks on tablets.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1057-2016 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2016-05-05 |
| Published | 2016-07-06 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Kvk Tech |
| Distribution | US |
Product
Benzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH, INC., Newtown, PA 18940, NDC 10702-0040-03
Reason
Discoloration: presence of scuffing marks on tablets.
Identifiers
| code_info | Lot #: 12825 A, 12937A, Exp 8/18 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
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Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1057-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.