DeRoyal Tonsillectomy Tray — Class II medical device recall Z-0906-2023
Terminated recall by DeRoyal Industries Inc, reported 2023-01-11, distributed in SC, VA. DeRoyal is recalling certain lots of surgical procedure pack products that contain a ConMed Foot Controlled El
| Recall number | Z-0906-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | DeRoyal Industries Inc, Powell, TN, United States |
| Recall initiated | 2022-11-28 |
| Classified | 2023-01-05 |
| Reported by FDA | 2023-01-11 |
| Terminated | 2026-03-18 |
| Distributed | SC, VA |
| Quantity | 320 units |
| UPC / GTIN / UDI-DI | 50749756373222 |
| Lot numbers | 57466936, 57897761 |
| Model numbers | 89-10698.01 |
| Expiration dates | 2026-06-01, 2026-08-01 |
Product
DeRoyal Tonsillectomy Tray, REF 89-10698.01
Reason for recall
DeRoyal is recalling certain lots of surgical procedure pack products that contain a ConMed Foot Controlled Electrosurgical Suction Coagulator. The recall is due to ConMed receiving reports that the suction ports may be occluded on the affected devices. If this occurs, the affected devices will not be able to perform the suction function during use.
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/Z-0906-2023. 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.