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.
Presence of Foreign Tablets/Capsules; A single foreign tablet Hydrochlorothiazide/Lisinopril 25/20 was found in one bottle
Rhodes Pharmaceuticals is recalling 10mg Oxycodone Hydrochloride Tablets because a single foreign tablet containing hydrochlorothiazide and lisinopril was found in one bottle. This could pose a risk if someone takes the foreign medication without knowing it.
The recall involves a single foreign tablet containing hydrochlorothiazide and lisinopril found in one bottle of Oxycodone. This could cause unintended medication interactions or side effects if taken without knowing it.
People who have the specific 100-count bottle of 10mg Oxycodone Hydrochloride Tablets with lot number WP5K0Y are affected. Those who take the medication as prescribed are most at risk if they accidentally consume the foreign tablets.
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.
Look for the lot number WP5K0Y and expiration date 02/28/2023 on the bottle.
The recall states a single foreign tablet was found in one bottle, so it is not safe to use without checking for the specific lot number.
The recall record does not mention a replacement or remedy.
The recall record does not specify a remedy, so contact Rhodes Pharmaceuticals directly for instructions.
We’ve drafted a message you can send Rhodes Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0794-2021 — Rhodes Pharmaceuticals Rhodes Pharmaceuticals Hello, I own a Rhodes Pharmaceuticals that is covered by recall D-0794-2021 from Rhodes Pharmaceuticals. 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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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.
