# FDA recall Z-0474-2023

> **ConMed Corporation** · Class II · device recall initiated 2022-11-18.

## 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.

## Distribution

Domestic distribution nationwide. Foreign distribution to Colombia, Ecuador, Nicaragua, Panama, Thailand, Australia, Canada, and Lebanon.

## Key facts

- **Recall number:** Z-0474-2023
- **Recalling firm:** ConMed Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-11-18
- **Report date:** 2022-12-21
- **Termination date:** 2026-04-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Utica, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0474-2023

## Citation

> AI Analytics. FDA recall Z-0474-2023. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/Z-0474-2023. Source: US FDA. Licensed CC0.

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