KVK-Tech, Inc.: 12 recalls on record

Recalls filed with 1 agency: FDA (12).

First recall on record: January 29, 2014. Most recent: May 28, 2025.

Risk classification: Class I: 2 · Class II: 5 · Class III: 5

Most recent recalls

DateAgencyProduct
May 28, 2025FDAPhentermine Hydrochloride Capsules, USP 30mg, 100-count bottle, Rx Only, Mfd. By: KVK-Tec…D-0446-2025
May 28, 2025FDAIndomethacin Extended-Release Capsules USP, 75 mg, 100-count bottle, Rx only, Mfd. By: KV…D-0445-2025
October 25, 2023FDABetaxolol Tablets, USP 10 mg, Rx Only, 100 count bottles, Mfd by: KVK Tech Inc., Newtown,…D-0049-2024
September 1, 2021FDAAtovaquone Oral Suspension, USP, 750 mg/5 mL, 210 mL bottle, Rx Only, Mfd. By: KVK-Tech, …D-0772-2021
May 26, 2021FDAHydrocodone Bitartrate and Homatropine Methlybromide tablets, USP, 5 mg/ 1.5 mg, 30-count…D-0386-2021
January 20, 2021FDABenzhydrocodone and Acetaminophen Tablets, CII, 6.12mg/ 325mg, 100 Tablets, Rx Only, Manu…D-0224-2021
October 23, 2019FDAMethylphenidate Hydrochloride Oral Solution 5mg per 5mL, 500 mL Bottle, Sugar Free Alcoho…D-0142-2020
August 23, 2017FDAPhentermine HCL Capsules, USP 15 mg, packaged in a) 100-count bottles (NDC 10702-026-01),…D-1083-2017
September 2, 2015FDAPhentermine Hydrochloride Capsules, USP, 15 mg, packaged in a) 100-count bottle (NDC 1070…D-1371-2015
January 29, 2014FDAHydrOXYzine HCI Tablets USP 50 mg, 100, 500, and 1000 count bottles, Rx only. Mfd by: KVK…D-1032-2014
January 29, 2014FDAHydrOXYzine HCI Tablets USP 25 mg, 100, 500, and 1000 count bottles, Rx only. Mfd by: KV…D-1031-2014
January 29, 2014FDAHydrOXYzine HCI Tablets USP 10 mg, 100 count bottles, Rx only. Mfd by KVK-TECH, INC, Newt…D-1030-2014

Questions about this company

How many recalls does KVK-Tech, Inc. have?
Recalert has 12 U.S. recalls on record for KVK-Tech, Inc., published between January 29, 2014 and May 28, 2025.
What was the most recent KVK-Tech, Inc. recall?
FDA recall D-0446-2025, published May 28, 2025: Phentermine Hydrochloride Capsules, USP 30mg, 100-count bottle, Rx Only, Mfd. By: KVK-Tech, Inc., Newtown, PA, 18940, Made in USA, NDC 10702-028-01.
Which agencies have handled KVK-Tech, Inc. recalls?
KVK-Tech, Inc. appears as the recalling firm in recalls from: FDA (12).

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