Drug recall
Betaxolol Tablets, USP 10 mg, Rx Only, 100 count bottles, Mfd by: KVK Tech Inc., Newtown, PA 18940, Made in…
FDA recall event 93101 · Class I · KVK-Tech, Inc.
Key facts
| Event ID | 93101 |
|---|---|
| Recall numbers | D-0049-2024 |
| Recalling firm | KVK-Tech, Inc. |
| Product type | Drugs |
| Products | Betaxolol Tablets, USP 10 mg, Rx Only, 100 count bottles, Mfd by: KVK Tech Inc., Newtown, PA 18940, Made in USA, NDC# 10702-013-01. |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Presence of Foreign Tablets/Capsules: There is a potential presence of oxycodone HCl tablets, USP 5 mg in bottles. |
| Initiation date | Sep 20, 2023 |
| Report date | Oct 25, 2023 |
| Termination date | Jul 29, 2025 |
| 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: