Oxycodone Hydrochloride Tablets — Class II drug recall D-0794-2021
Terminated recall by Rhodes Pharmaceuticals, L.P., reported 2021-09-22, distributed nationwide. Presence of Foreign Tablets/Capsules; A single foreign tablet Hydrochlorothiazide/Lisinopril 25/20 was found i
| Recall number | D-0794-2021 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Rhodes Pharmaceuticals, L.P., Coventry, RI, United States |
| Recall initiated | 2021-08-19 |
| Classified | 2021-09-13 |
| Reported by FDA | 2021-09-22 |
| Terminated | 2023-03-07 |
| Distributed | Nationwide (US) |
| Quantity | 55,344 |
| NDC | 42858-0001, 42858-0001-01, 42858-0001-10, 42858-0002, 42858-0002-01, 42858-0002-10, 42858-0003, 42858-0003-01, 42858-0004, 42858-0004-01, 42858-0005, 42858-0005-01 |
| Lot numbers | WP5K0Y |
| Expiration dates | 2023-02-28 |
Product
Oxycodone Hydrochloride Tablets, USP, 10 mg, 100 count bottle, Rx only, Marketed by: Rhodes Pharmaceuticals L.P., Coventry RI 02816, Manufactured by: Purdue Pharma L.P., Stanford, CT 06901 NDC 42858-002-01
Reason for recall
Presence of Foreign Tablets/Capsules; A single foreign tablet Hydrochlorothiazide/Lisinopril 25/20 was found in one bottle
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0794-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.