Foot Controlled Electrosurgical Suction Coagulator — Class II medical device recall Z-0474-2023
Terminated recall by ConMed Corporation, reported 2022-12-21, distributed nationwide. Suction ports may potentially be occluded on the affected devices. If this occurs, the affected devices will n
| Recall number | Z-0474-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ConMed Corporation, Utica, NY, United States |
| Recall initiated | 2022-11-18 |
| Classified | 2022-12-09 |
| Reported by FDA | 2022-12-21 |
| Terminated | 2026-04-13 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, CO, EC, LB, NI, PA, TH |
| UPC / GTIN / UDI-DI | 30653405059930 |
| Lot numbers | 202204294, 202205134, 202205164, 202206084, 202206154, 202206204, 202206304, 202207074, 202207084, 202208014, 202208044, 202208084 |
| Model numbers | 130187 |
Product
Foot Controlled Electrosurgical Suction Coagulator, Electrosurgical Suction Coagulator 10FR, Catalog Number 130187
Reason for recall
Suction ports may potentially be occluded on the affected devices. If this occurs, the affected devices will not be able to perform the suction function during use, which could cause a delay in procedure and could require another device to be used.
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-0474-2023. 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.