PlainRecalls
FDA Drug Critical Class I Terminated

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.

Reported: October 25, 2023 Initiated: September 20, 2023 #D-0049-2024

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.

Reason for Recall

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

Details

Recalling Firm
KVK-Tech, Inc.
Units Affected
1488 bottles
Distribution
Nationwide in the USA and PR
Location
Newtown, PA

Frequently Asked Questions

What product was recalled?
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.. Recalled by KVK-Tech, Inc.. Units affected: 1488 bottles.
Why was this product recalled?
Presence of Foreign Tablets/Capsules: There is a potential presence of oxycodone HCl tablets, USP 5 mg in bottles.
Which agency issued this recall?
This recall was issued by the FDA Drug on October 25, 2023. Severity: Critical. Recall number: D-0049-2024.