DeRoyal recalls certain tonsillectomy trays with suction ports that may become clogged, preventing suction function during surgery. Affected units have specific lot numbers and expiration dates.
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.
DeRoyal is recalling tonsillectomy trays that may have clogged suction ports, which could prevent proper suction during surgery. This is a safety issue for medical procedures requiring the device.
The suction ports in certain lots of the DeRoyal Tonsillectomy Tray may become blocked during use. If blocked, the device cannot perform suction, which is critical for removing blood and fluids during surgery.
Healthcare professionals using the DeRoyal Tonsillectomy Tray for surgical procedures are most at risk. Patients undergoing tonsillectomy surgery may be affected if the device is used on an affected unit.
Check the lot number on the tray: Lot 57466936 (expires 8/1/2026) or Lot 57897761 (expires 6/1/2026). The product is sold under the DeRoyal brand with the reference number 89-10698.01.
Ensure the suction ports work properly by testing for suction before use in a surgical setting.
Lot 57466936 (expires 8/1/2026) and Lot 57897761 (expires 6/1/2026).
ConMed reports that suction ports may become occluded on these devices, preventing suction function during surgery.
The recall does not specify a fix; users must check if suction ports are working and avoid using affected units.
We’ve drafted a message you can send DeRoyal to request your refund or repair — edit it as you like.
Subject: Recall Z-0906-2023 — DeRoyal DeRoyal Hello, I own a DeRoyal that is covered by recall Z-0906-2023 from DeRoyal. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
