Lower riskDrug recall · FDA · Published August 19, 2021
Rhodes Pharmaceuticals recalls 10mg Oxycodone tablets with foreign medication
Rhodes Pharmaceuticals recalls 10mg Oxycodone tablets due to foreign hydrochlorothiazide/lisinopril tablets found in one batch. Consumers should check their bottles for the specific lot number and contact the company for details.
“Rhodes Pharmaceuticals recalls 10mg Oxycodone tablets with foreign medication.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/35930-rhodes-pharmaceuticals-recalls-10mg-oxycodone-tablets-with-foreign-medication. Based on FDA recall #D-0794-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0794-2021%22&limit=1).
The FDA announced on Aug. 19, 2021, that Rhodes Pharmaceuticals L.P. is recalling Oxycodone Hydrochloride Tablets USP, 10 mg, due to the presence of foreign tablets. The agency said a single bottle contained a Hydrochlorothiazide/Lisinopril tablet.
The recall is due to the presence of foreign tablets in one bottle. The FDA said a single Hydrochlorothiazide/Lisinopril 25/20 tablet was found in one bottle of Oxycodone Hydrochloride Tablets.
Context
GovInfoNow's records show Rhodes Pharmaceuticals, L.P. has one other recall on record since April 17, 2018, for Aptensio XR capsules regarding failed dissolution specifications. Other recent recalls of similar products include Glenmark Bisoprolol/Hydrochlorothiazide Tablets Recall (Nov. 21, 2025), Granules Pharmaceuticals Trazodone 50mg Recall (Jan. 26, 2026), and Amerisource Health Primidone Tablets Recall (May 1, 2026).
How to tell if you have this one
Check your Oxycodone Hydrochloride Tablets, USP, 10mg, 100-count bottle for the lot number WP5K0Y and expiration date 02/28/2023. The product is only available by prescription.
Brand
Rhodes Pharmaceuticals
Category
Drug
Based on the official FDA remedy
What to do — step by step
Check Your Product
Look for the lot number WP5K0Y and expiration date 02/28/2023 on the bottle.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Product was distributed nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 19 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
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-0794-2021 (August 19, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0794-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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.