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.
Lower-risk recall
Labeling: Wrong bar code
Contact the company & request your remedy
What happened, in plain English
KVK-Tech is recalling 500-count Oxybutynin Chloride Tablets (5mg) because they have a wrong bar code. This labeling issue could cause confusion in prescription handling but does not create a safety risk for users. Read more at govinfonow.com/recall/39373-kvk-tech-oxybutynin-tablets-wrong-bar-code-labeling-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/39373-kvk-tech-oxybutynin-tablets-wrong-bar-code-labeling-hazard · Updated October 5, 2026 · FDA enforcement record: FDA #D-0340-2019
Cite this page
“KVK-Tech Oxybutynin Tablets: Wrong Bar Code Labeling Hazard.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/39373-kvk-tech-oxybutynin-tablets-wrong-bar-code-labeling-hazard. Based on FDA recall #D-0340-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0340-2019%22&limit=1).
Why it’s dangerous
The product has a wrong bar code, which could lead to confusion during prescription processing. However, this does not create a safety risk for end users.
Who’s affected
Prescription patients who have the 500-count Oxybutynin Chloride Tablets (5mg) from KVK-Tech. Those most at risk are pharmacy staff handling the product.
How to tell if you have this one
Check for the 500-count bottle labeled 'Oxybutynin Chloride Tablets, USP, 5 mg' with manufacturer KVK-Tech, Inc. from Newtown, PA. The specific lot number is 15079A, expiring 10/2020.
- Brand
KVK-Tech- Category
Drug
What to do — step by step
Check Product Label
Look for the 500-count bottle with the correct product name and manufacturer details.
Questions people ask
Is this product dangerous to use?
No, the wrong bar code does not pose a safety risk. This is a labeling issue that could cause confusion in prescription handling but does not affect user safety.
What should I do if I have this product?
The recall does not require action. You can continue using the product as it is safe.
How can I tell if I have the recalled product?
Check for the 500-count bottle labeled 'Oxybutynin Chloride Tablets, USP, 5 mg' with manufacturer KVK-Tech, Inc. from Newtown, PA. The specific lot number is 15079A, expiring 10/2020.
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-0340-2019 — KVK-Tech KVK-Tech Hello, I own a KVK-Tech that is covered by recall D-0340-2019 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-0340-2019 (December 11, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0340-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 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.