# FDA recall Z-0906-2023

> **DeRoyal Industries Inc** · Class II · device recall initiated 2022-11-28.

## 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.

## Distribution

Distribution in US states of VA, and SC.

## Key facts

- **Recall number:** Z-0906-2023
- **Recalling firm:** DeRoyal Industries Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-11-28
- **Report date:** 2023-01-11
- **Termination date:** 2026-03-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Powell, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0906-2023

## Citation

> AI Analytics. FDA recall Z-0906-2023. Retrieved 2026-08-18 from https://api.ai-analytics.org/recall/Z-0906-2023. Source: US FDA. Licensed CC0.

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