FDA Drug Recalls

Recalls / Firms / KVK Tech, Inc.

KVK Tech, Inc.

15 FDA drug recalls on record2 Class I.

DateClassDrugStatus
2025-05-09Class IIPhentermine HydrochlorideOngoing
2025-05-09Class IIIndomethacinOngoing
2023-09-20Class IBetaxolol HydrochlorideTerminated
2021-07-02Class IAtovaquone Oral SuspensionTerminated
2021-04-27Class IIIHydrocodone Bitartrate And Homatropine MethylbromideTerminated
2020-12-18Class IIIBenzhydrocodone and Acetaminophen Tablets, CII, 6.12mg/ 325mg, 100 Tablets, Rx Only, ManufTerminated
2019-11-01Class IIHydrocodone Bitartrate And Homatropine MethylbromideTerminated
2019-10-04Class IIIMethylphenidate Hydrochloride Oral Solution 5mg per 5mL, 500 mL Bottle, Sugar Free AlcoholTerminated
2018-12-11Class IIOxybutynin ChlorideTerminated
2017-08-03Class IIIPhentermine HydrochlorideTerminated
2016-05-05Class IIIBenzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH, INTerminated
2015-07-14Class IIIPhentermine Hydrochloride Capsules, USP, 15 mg, packaged in a) 100-count bottle (NDC 10702Terminated
2013-12-11Class IIHydroxyzine HydrochlorideTerminated
2013-12-11Class IIHydroxyzine HydrochlorideTerminated
2013-12-11Class IIHydroxyzine HydrochlorideTerminated