“KVK Tech Betaxolol Tablets Recall: Risk of Oxycodone Contamination.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/33129-kvk-tech-betaxolol-tablets-recall-risk-of-oxycodone-contamination. Based on FDA recall #D-0049-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0049-2024%22&limit=1).
The FDA announced on Sept. 20, 2023, that KVK Tech, Inc. voluntarily recalled Betaxolol Tablets, USP 10 mg due to the potential presence of oxycodone HCl tablets in the bottles. The recall affects 1,488 bottles distributed nationwide.
The recall is due to the potential presence of oxycodone HCl tablets, USP 5 mg in bottles of Betaxolol Tablets, USP 10 mg. The FDA classified this as a Class I recall.
Context
GovInfoNow's records show KVK Tech, Inc. has 11 other recalls on record since Dec. 11, 2013. Other recent recalls of similar products include SpecGx Oxycodone/Acetaminophen Tablets Recall (Dec. 16, 2025), Oxycodone 5mg Tablets Recall (Jan. 14, 2026), and Unichem Bisoprolol/Hydrochlorothiazide Tablets Recall (Jan. 21, 2026).
How to tell if you have this one
Check for the lot number 17853A on the bottle label. The product is a 100-count Betaxolol 10mg tablet bottle made in the USA by KVK Tech in Newtown, PA. The expiration date is June 30, 2027.
Brand
KVK Tech
Category
Drug
Based on the official FDA remedy
What to do — step by step
Stop Using Now
Immediately stop using the recalled Betaxolol tablets if you have them. Do not take any tablets from this lot.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Nationwide in the USA and PR” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 22 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0049-2024 (September 20, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0049-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.