Recalling firm
KVK-Tech, Inc.
Product type
Drug
Status
Terminated
Report date
2023-10-25
Distribution
Nationwide in the USA and PR
Firm state
PA
Product quantity
1488 bottles
Initiated by
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.
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.
Code / lot info
Lot # 17853A, Exp. 06/30/2027
Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.