Drug recall
Benzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH, INC., Newtown, PA…
FDA recall event 74086 · Class III · KVK-Tech, Inc.
Key facts
| Event ID | 74086 |
|---|---|
| Recall numbers | D-1057-2016 |
| Recalling firm | KVK-Tech, Inc. |
| Product type | Drugs |
| Products | Benzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH, INC., Newtown, PA 18940, NDC 10702-0040-03 |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Discoloration: presence of scuffing marks on tablets. |
| Initiation date | May 5, 2016 |
| Report date | Jul 6, 2016 |
| Termination date | Jan 13, 2017 |
| City | Newtown |
| State | PA |
| Country | United States |
| FEI number | 3005117563 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: