KVK Tech Recalls
15 recalls on record · January 29, 2014 to May 28, 2025 · Drugs
Recalls by year
14
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16
17
18
19
21
23
25
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
May 28, 2025DrugsFDA
KVK Tech, Inc. recalls Phentermine Hydrochloride Capsules, USP 30mg, 100-count bottle, Rx Only, Mfd. By: KVK-Tech, Inc., Newtown, PA, 18940, Ma
Hazard: cGMP deviations
May 28, 2025DrugsFDA
KVK Tech, Inc. recalls Indomethacin Extended-Release Capsules USP, 75 mg, 100-count bottle, Rx only, Mfd. By: KVK-Tech, Inc., Newtown, PA, 1894
Hazard: cGMP deviations
October 25, 2023DrugsFDA
KVK-Tech, Inc. recalls Betaxolol Tablets, USP 10 mg, Rx Only, 100 count bottles, Mfd by: KVK Tech Inc., Newtown, PA 18940, Made in USA, NDC# 10
Hazard: Presence of Foreign Tablets/Capsules: There is a potential presence of oxycodone HCl tablets, USP 5 mg in bottles.
September 1, 2021DrugsFDA
KVK-Tech, Inc. recalls Atovaquone Oral Suspension, USP, 750 mg/5 mL, 210 mL bottle, Rx Only, Mfd. By: KVK-Tech, Inc., Newtown, PA 18940, NDC 1
Hazard: Temperature abuse: the firm received customer complaints of unusual grittiness in the product.
May 26, 2021DrugsFDA
KVK-Tech, Inc. recalls Hydrocodone Bitartrate and Homatropine Methlybromide tablets, USP, 5 mg/ 1.5 mg, 30-count bottle, Rx only, Mfd. By:KVK-T
Hazard: Failed Impurities/Degradation Specifications
January 20, 2021DrugsFDA
KVK-Tech, Inc. recalls Benzhydrocodone and Acetaminophen Tablets, CII, 6.12mg/ 325mg, 100 Tablets, Rx Only, Manufactured for: KVK-Tech, Inc., N
Hazard: Failed Impurities/Degradation Specifications; out of specification results obtained for N-Oxide impurity during the 12-month long term stability testing for Batch# 15892A
November 20, 2019DrugsFDA
KVK-Tech, Inc. recalls Hydrocodone Bitartrate and Homatropine Methlybromide Oral Solution 5 mg/1.5 mg per 5 mL, 473 mL bottles, Rx only, Mfd. b
Hazard: Presence of Foreign Substance: Black particles were found in the lots during retain sample inspection
October 23, 2019DrugsFDA
KVK-Tech, Inc. recalls Methylphenidate Hydrochloride Oral Solution 5mg per 5mL, 500 mL Bottle, Sugar Free Alcohol Free, Rx Only, Mfd by: KVK Te
Hazard: Presence of Foreign Substance; Fiber particles.
December 26, 2018DrugsFDA
KVK-Tech, Inc. recalls Oxybutynin Chloride Tablets, USP, 5 mg, 500-count bottle, Rx only, Mfd. By: KVK-Tech, Inc., Newtown, PA 18940, NDC 10702
Hazard: Labeling: Wrong bar code
August 23, 2017DrugsFDA
KVK-Tech, Inc. recalls Phentermine HCL Capsules, USP 15 mg, packaged in a) 100-count bottles (NDC 10702-026-01), and b) 1000-count bottles (NDC
Hazard: Failed Impurities/Degradation Specifications: out-of-specification results obtained for individual unknown impurities found at 30 month Room Temperature Retained Sample stability test.
July 6, 2016DrugsFDA
KVK-Tech, Inc. recalls Benzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH, INC., Newtown, PA 18940, NDC 107
Hazard: Discoloration: presence of scuffing marks on tablets.
September 2, 2015DrugsFDA
KVK-Tech, Inc. recalls Phentermine Hydrochloride Capsules, USP, 15 mg, packaged in a) 100-count bottle (NDC 10702-0026-01; UPC 3 10702 02601 8)
Hazard: Failed Impurities/Degradation Specifications: out-of-specification results for individual unknown and total impurity at the 12th month room temperature stability test station
January 29, 2014DrugsFDA
KVK-Tech, Inc. recalls HydrOXYzine HCI Tablets USP 50 mg, 100, 500, and 1000 count bottles, Rx only. Mfd by: KVK-TECH, INC, Newtown, PA 18940.
Hazard: Good Manufacturing Practices Deviations: The product has an Active Pharmaceutical Ingredient from an unapproved source.
January 29, 2014DrugsFDA
KVK-Tech, Inc. recalls HydrOXYzine HCI Tablets USP 25 mg, 100, 500, and 1000 count bottles, Rx only. Mfd by: KVK-TECH, INC, Newtown, PA 18940.
Hazard: Good Manufacturing Practices Deviations: The product has an Active Pharmaceutical Ingredient from an unapproved source.
January 29, 2014DrugsFDA
KVK-Tech, Inc. recalls HydrOXYzine HCI Tablets USP 10 mg, 100 count bottles, Rx only. Mfd by KVK-TECH, INC, Newtown, PA 18940. NDC #10702-010-
Hazard: Good Manufacturing Practices Deviations: The product has an Active Pharmaceutical Ingredient from an unapproved source.