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.
Recall notice
Failed Impurities/Degradation Specifications
Contact the company & request your remedy
What happened, in plain English
KVK-Tech is recalling 5 mg/1.5 mg hydrocodone bitartrate and homatropine methlybromide tablets due to failed impurities and degradation specifications. This recall affects prescription-only products that may pose health risks if used as intended. Read more at govinfonow.com/recall/36190-kvk-tech-hydrocodone-tablets-recall-impurities-may-cause-harm.
Source Summary by GovInfoNow · govinfonow.com/recall/36190-kvk-tech-hydrocodone-tablets-recall-impurities-may-cause-harm · Updated October 4, 2026 · FDA enforcement record: FDA #D-0386-2021
Cite this page
“KVK-Tech Hydrocodone Tablets Recall: Impurities May Cause Harm.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36190-kvk-tech-hydrocodone-tablets-recall-impurities-may-cause-harm. Based on FDA recall #D-0386-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0386-2021%22&limit=1).
Why it’s dangerous
The tablets failed impurities and degradation specifications, meaning they may contain harmful substances that could cause health issues when taken. This is a prescription-only product that requires medical supervision.
Who’s affected
Prescription holders of the 30-count hydrocodone tablets with NDC 10702-055-03 and lot 15684A. People using these specific prescription medications are most at risk.
How to tell if you have this one
Check for the NDC code 10702-055-03 and lot number 15684A on the product label. The product is a prescription-only 30-count bottle of hydrocodone tablets.
- Brand
KVK-Tech- Category
Drug
What to do — step by step
Check Product Details
Look for NDC 10702-055-03 and lot 15684A on the label.
Questions people ask
Is this product safe to use?
The recall states the product failed impurities and degradation specifications, but does not specify if it is safe to use. The manufacturer recommends checking the recall details.
What should I do if I have this product?
The recall record does not provide a remedy or action steps for affected products.
How can I confirm if my product is recalled?
Check the NDC code 10702-055-03 and lot number 15684A on the product label.
Contact KVK-Tech
We’ve drafted a message you can send KVK-Tech to request your refund or repair — edit it as you like.
Subject: Recall D-0386-2021 — KVK-Tech KVK-Tech Hello, I own a KVK-Tech that is covered by recall D-0386-2021 from KVK-Tech. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0386-2021 (April 27, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0386-2021 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.