KVK Tech, Inc. recalls
Every recall we track for KVK Tech, Inc. — 15 in all, from 2013–2025 — plus the complaints and injury reports the public filed about them. 2 are rated “stop using now”.
Recalls per year, by danger level
10 recalls since 2017. 20% rated “stop using now”.
All FDA recall records for KVK Tech, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 1 | 0 | 1 |
| 2018 | 0 | 0 | 1 | 0 | 1 |
| 2019 | 1 | 1 | 0 | 0 | 2 |
| 2020 | 0 | 1 | 0 | 0 | 1 |
| 2021 | 0 | 0 | 1 | 1 | 2 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 1 | 0 | 0 | 0 | 1 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 2 | 2 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
KVK Tech, Inc. recalls before 2017
Recalls on record by year.
Most common reasons for KVK Tech, Inc. recalls
What to do if you have a recalled KVK Tech, Inc. product
- Match the NDC and lot number on your bottle or box to the recall.
- Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first.
- Report side effects to FDA MedWatch.
All KVK Tech, Inc. recalls
12 shown- UnratedDrug
KVK Tech, Inc. recalls Indomethacin Extended-Release Capsules USP, 75 mg, 100-count bottle, Rx only, Mfd. By: KVK-Tech, Inc., Newtown, PA,
KVK Tech recalls 75mg Indomethacin Extended-Release Capsules (NDC 10702-016-01) made in USA with cGMP deviations. Consumers should contact the manufacturer for details.
KVK TechMay 9, 2025 - Stop using nowDrug
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#
KVK Tech recalls 100-count Betaxolol 10mg tablets (Rx only) due to potential oxycodone contamination. Affected lots may contain dangerous opioid tablets.
KVK TechSep 20, 2023 - Lower riskDrug
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
KVK-Tech recalls Atovaquone Oral Suspension (750 mg/5 mL, 210 mL) due to customer reports of unusual grittiness. This medication is prescription-only and may be affected by specific batch numbers.
KVK-TechJul 2, 2021 - UnratedDrug
KVK-Tech, Inc. recalls Hydrocodone Bitartrate and Homatropine Methlybromide tablets, USP, 5 mg/ 1.5 mg, 30-count bottle, Rx only, Mfd.
KVK-Tech recalls 5mg/1.5mg hydrocodone tablets with impurities that could cause harm. Rx-only product from Newtown, PA. Check NDC 10702-055-03 and lot 15684A.
KVK-TechApr 27, 2021 - Use cautionDrug
KVK-Tech, Inc. recalls Benzhydrocodone and Acetaminophen Tablets, CII, 6.12mg/ 325mg, 100 Tablets, Rx Only, Manufactured for: KVK-Tech, Inc.,
KVK-Tech recalls Batch 15892A of Benzhydrocodone and Acetaminophen Tablets due to failed impurity specifications. Check your bottle's lot number.
KVK-TechDec 18, 2020 - Stop using nowDrug
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.
KVK-Tech recalls specific lots of Hydrocodone Bitartrate and Homatropine Methylobromide Oral Solution due to black particles found in the liquid.
KVK-TechNov 1, 2019 - Use cautionDrug
KVK-Tech, Inc. recalls Methylphenidate Hydrochloride Oral Solution 5mg per 5mL, 500 mL Bottle, Sugar Free Alcohol Free, Rx Only, Mfd by: KVK
KVK-Tech recalls 384 bottles of Methylphenidate Hydrochloride Oral Solution due to fiber particles. Check your batch and expiration date.
KVK-TechOct 4, 2019 - Lower riskDrug
KVK-Tech, Inc. recalls Oxybutynin Chloride Tablets, USP, 5 mg, 500-count bottle, Rx only, Mfd. By: KVK-Tech, Inc., Newtown, PA 18940, NDC
KVK-Tech recalls 500-count Oxybutynin Chloride Tablets (5mg) due to incorrect bar code labeling. This may cause confusion in prescription handling but does not pose a safety risk.
KVK-TechDec 11, 2018 - Lower riskDrug
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
KVK Tech recalls 100-count and 1000-count 15mg Phentermine capsules due to impurities found in stability testing. These capsules may pose a risk of serious injury if taken.
KVK TechAug 3, 2017 - UnratedDrug
KVK-Tech, Inc. recalls Benzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH, INC., Newtown, PA 18940, NDC
KVK-Tech recalls specific lots of 50 mg Benzphetamine tablets due to scuffing marks and discoloration. Check your bottle's lot number.
KVK-TechMay 5, 2016 - Use cautionDrug
KVK-Tech, Inc. recalls Phentermine Hydrochloride Capsules, USP, 15 mg, packaged in a) 100-count bottle (NDC 10702-0026-01; UPC 3 10702 02601
KVK-Tech recalls 15 mg Phentermine capsules due to failed impurity specifications. Check your lot numbers and expiration dates for affected batches.
KVK-TechJul 14, 2015 - Use cautionDrug
KVK-Tech, Inc. recalls HydrOXYzine HCI Tablets USP 10 mg, 100 count bottles, Rx only. Mfd by KVK-TECH, INC, Newtown, PA 18940. NDC
KVK-Tech recalls 10mg Hydroxyzine HCl tablets because the active ingredient came from an unapproved source. Check your lot number.
KVK-TechDec 11, 2013
KVK Tech, Inc. recall questions
How many recalls has KVK Tech, Inc. had?
15 recalls from KVK Tech, Inc. are on record with U.S. safety agencies, from 2013–2025.
What is the most recent KVK Tech, Inc. recall?
KVK Tech, Inc. recalls Indomethacin Extended-Release Capsules USP, 75 mg, 100-count bottle, Rx only, Mfd. By: KVK-Tech, Inc., Newtown, PA,, dated May 9, 2025. Every KVK Tech, Inc. recall is listed on this page, newest first.
Why are KVK Tech, Inc. products recalled?
The most common reasons on record: cGMP deviations (2).
What should I do if I have a recalled KVK Tech, Inc. product?
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
How do I get alerts for new KVK Tech, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.