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.

FDA recall notice · announced October 25, 2023 · Kvk-tech

Class I FDA/FSIS Class I: reasonable probability that use will cause serious adverse health consequences or death.

The product

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.

Reason for recall

Presence of Foreign Tablets/Capsules: There is a potential presence of oxycodone HCl tablets, USP 5 mg in bottles.

Notes

Distribution: Nationwide in the USA and PR
Lot/code information: Lot # 17853A, Exp. 06/30/2027
Quantity: 1488 bottles
Status: Terminated
Products in this recall event:
- 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. (D-0049-2024)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.