--- title: "KVK-Tech, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search KVK-Tech, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/kvk-tech-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # KVK-Tech, Inc. recall records **2** reported ongoing 4 records in this archive. Latest source date May 9, 2025. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status May 9, 2025 FDA drug enforcement ### [Indomethacin Extended-Release Capsules USP, 75 mg, 100-count bottle, Rx only, Mfd. By: KVK-Tech, Inc., Newtown, PA, 18940, Made in USA, NDC 10702-016-01.](https://isitonrecall.com/recall/fda-drug-d-0445-2025-indomethacin-extended-release-capsules-usp-75-mg-100-count-bottle-rx-only-mfd-by-kvk-tech-inc-newtow/) cGMP deviations Class II Reported ongoing Distribution: Nationwide [Official source for Indomethacin Extended-Release Capsules USP, 75 mg, 100-count bottle, Rx only, Mfd. By: KVK-Tech, ...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0445-2025%22) May 9, 2025 FDA drug enforcement ### [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.](https://isitonrecall.com/recall/fda-drug-d-0446-2025-phentermine-hydrochloride-capsules-usp-30mg-100-count-bottle-rx-only-mfd-by-kvk-tech-inc-newtown-pa/) cGMP deviations Class II Reported ongoing Distribution: Nationwide [Official source for Phentermine Hydrochloride Capsules, USP 30mg, 100-count bottle, Rx Only, Mfd. By: KVK-Tech, Inc.,...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0446-2025%22) Oct 3, 2023 FDA company announcement ### [KVK Tech: Betaxolol Tablets, USP](https://isitonrecall.com/recall/fdapress-f81f73f8b37316b1-kvk-tech-betaxolol-tablets-usp/) Potential Presence of Oxycodone HCl tablet Not supplied Reported terminated Distribution: KVK notified its distributors and customers by a Recall Notification Letter via email and FedEx overnight mail on 09/26/2023 and is arranging for the return of all recalled prod... [Official source for KVK Tech: Betaxolol Tablets, USP](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/kvk-tech-inc-issues-voluntary-nationwide-recall-one-lot-betaxolol-tablets-usp-10-mg-batch-number) Sep 20, 2023 FDA drug enforcement ### [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.](https://isitonrecall.com/recall/fda-drug-d-0049-2024-betaxolol-tablets-usp-10-mg-rx-only-100-count-bottles-mfd-by-kvk-tech-inc-newtown-pa-18940-made-in-u/) Presence of Foreign Tablets/Capsules: There is a potential presence of oxycodone HCl tablets, USP 5 mg in bottles. Class I Reported terminated Distribution: Nationwide in the USA and PR [Official source for Betaxolol Tablets, USP 10 mg, Rx Only, 100 count bottles, Mfd by: KVK Tech Inc., Newtown, PA 1894...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0049-2024%22) ## Reasons in these listed records - cGMP deviations - Potential Presence of Oxycodone HCl tablet - Presence of Foreign Tablets/Capsules: There is a potential presence of oxycodone HCl tablets, USP 5 mg in bottles. These examples come from this result page and are not a ranking of every recall reason. ## Checking KVK-Tech, Inc. ### Is there a recall on kvk-tech, inc. right now? This archive contains 4 records, including 2 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search KVK-Tech, Inc.](https://isitonrecall.com/check/?q=KVK-Tech%2C%20Inc.) 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