KVK-Tech, Inc.: Drug Recall
Recall #D-0049-2024 · 09/20/2023
Class I: Dangerous
Recall Details
- Recall Number
- D-0049-2024
- Classification
- Class I
- Product Type
- Drug
- Recalling Firm
- KVK-Tech, Inc.
- Status
- Terminated
- Date Initiated
- 09/20/2023
- Location
- Newtown, PA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1488 bottles
Reason for Recall
Presence of Foreign Tablets/Capsules: There is a potential presence of oxycodone HCl tablets, USP 5 mg in bottles.
Product Description
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.
Distribution Pattern
Nationwide in the USA and PR
Other Recalls by KVK-Tech, Inc.
- Class II: Risk 05/09/2025
- Class II: Risk 05/09/2025
- Class I: Dangerous 07/02/2021
- Class III: Low Risk 04/27/2021
- Class III: Low Risk 12/18/2020
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.