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DeRoyal 89-10698Recalls & reported problems

Deroyal Industries, Inc. · TONSILLECTOMY TRAY · Class 1

Data updated Oct 13, 2026 from official FDA records · Editorial policy

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Nov 28, 2022Terminated

    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.

    Z-0906-2023 · Root cause: Nonconforming Material/Component · FDA record ↗

Other Ear, nose, and throat surgical tray devices

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Sources and updates

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