Kvk Tech recalls
Kvk Tech appears in 15 official U.S. recall notices indexed by RecallRadar, most recently on 2025-05-28.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 15 |
|---|---|
| Published | 2014-01-29 to 2025-05-28 |
| By agency | FDA Drug (15) |
| By classification | Class II (7), Class III (6), Class I (2) |
| By status | terminated (13), ongoing (2) |
| Distribution named in notices | US |
Recalls
- Indomethacin Extended-Release Capsules USP, 75 mg, 100-count bottle, Rx only, Mfd
FDA Drug · Class II · 2025-05-28 · Kvk Tech
Reason: cGMP deviations - Phentermine Hydrochloride Capsules, USP 30mg, 100-count bottle, Rx Only, Mfd
FDA Drug · Class II · 2025-05-28 · Kvk Tech
Reason: cGMP deviations - 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 Drug · Class I · 2023-10-25 · Kvk Tech
Reason: Presence of Foreign Tablets/Capsules: There is a potential presence of oxycodone HCl tablets, USP 5 mg in bottles. - Atovaquone Oral Suspension, USP, 750 mg/5 mL, 210 mL bottle, Rx Only, Mfd
FDA Drug · Class I · 2021-09-01 · Kvk Tech
Reason: Temperature abuse: the firm received customer complaints of unusual grittiness in the product. - Hydrocodone Bitartrate and Homatropine Methlybromide tablets, USP, 5 mg/ 1.5 mg, 30-count bottle, Rx only, Mfd
FDA Drug · Class III · 2021-05-26 · Kvk Tech
Reason: Failed Impurities/Degradation Specifications - Benzhydrocodone and Acetaminophen Tablets, CII, 6.12mg/ 325mg, 100 Tablets, Rx Only, Manufactured for: KVK-Tech, Inc., Newtown, PA 18940 US…
FDA Drug · Class III · 2021-01-20 · Kvk Tech
Reason: Failed Impurities/Degradation Specifications; out of specification results obtained for N-Oxide impurity during the 12-month long term stability testing for Batch# 15892A - Hydrocodone Bitartrate and Homatropine Methlybromide Oral Solution 5 mg/1.5 mg per 5 mL, 473 mL bottles, Rx only, Mfd. by: KVK-Tech, Inc
FDA Drug · Class II · 2019-11-20 · Kvk Tech
Reason: Presence of Foreign Substance: Black particles were found in the lots during retain sample inspection - Methylphenidate Hydrochloride Oral Solution 5mg per 5mL, 500 mL Bottle, Sugar Free Alcohol Free, Rx Only, Mfd by: KVK Tech, Inc., Newtown,…
FDA Drug · Class III · 2019-10-23 · Kvk Tech
Reason: Presence of Foreign Substance; Fiber particles. - Oxybutynin Chloride Tablets, USP, 5 mg, 500-count bottle, Rx only, Mfd
FDA Drug · Class II · 2018-12-26 · Kvk Tech
Reason: Labeling: Wrong bar code - Phentermine HCL Capsules, USP 15 mg, packaged in a) 100-count bottles (NDC 10702-026-01), and b) 1000-count bottles (NDC 10702-026-10), Rx…
FDA Drug · Class III · 2017-08-23 · Kvk Tech
Reason: Failed Impurities/Degradation Specifications: out-of-specification results obtained for individual unknown impurities found at 30 month Room Temperature Retained Sample stability test. - Benzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH, INC., Newtown, PA 18940, NDC 10702-0040-03
FDA Drug · Class III · 2016-07-06 · Kvk Tech
Reason: Discoloration: presence of scuffing marks on tablets. - Phentermine Hydrochloride Capsules, USP, 15 mg, packaged in a) 100-count bottle (NDC 10702-0026-01
FDA Drug · Class III · 2015-09-02 · Kvk Tech
Reason: Failed Impurities/Degradation Specifications: out-of-specification results for individual unknown and total impurity at the 12th month room temperature stability test station - HydrOXYzine HCI Tablets USP 10 mg, 100 count bottles, Rx only
FDA Drug · Class II · 2014-01-29 · Kvk Tech
Reason: Good Manufacturing Practices Deviations: The product has an Active Pharmaceutical Ingredient from an unapproved source. - HydrOXYzine HCI Tablets USP 25 mg, 100, 500, and 1000 count bottles, Rx only
FDA Drug · Class II · 2014-01-29 · Kvk Tech
Reason: Good Manufacturing Practices Deviations: The product has an Active Pharmaceutical Ingredient from an unapproved source. - HydrOXYzine HCI Tablets USP 50 mg, 100, 500, and 1000 count bottles, Rx only
FDA Drug · Class II · 2014-01-29 · Kvk Tech
Reason: Good Manufacturing Practices Deviations: The product has an Active Pharmaceutical Ingredient from an unapproved source.