Lutronic recalls XERF EFFECTOR 60 electrosurgical units made between April 2025 and August 2025 due to rare patient adverse events from manufacturing defects.
Manufacturing defects in devices manufactured from 4/1/25 to 8/20/25 can on rare occasions result in adverse events for patients.
Lutronic is recalling XERF EFFECTOR 60 electrosurgical units produced from April to August 2025 because manufacturing defects may cause rare patient adverse events. This recall affects medical professionals using these devices for surgical procedures.
Manufacturing defects in the electrosurgical units can, on rare occasions, lead to adverse events for patients during surgery. The defect occurs in the devices produced between April 2025 and August 2025.
Medical professionals who use the XERF EFFECTOR 60 electrosurgical unit for surgical procedures are most at risk. Patients receiving surgery with these devices may experience rare adverse events.
Check for model numbers 1101210000, 1101210100, or 1101210200. Devices manufactured from April 1, 2025 to August 20, 2025 are affected.
Verify the model number and production date against the listed identifiers to confirm if the device is affected.
Lutronic recalls XERF EFFECTOR 60 electrosurgical units made between April 2025 and August 2025 due to manufacturing defects that may cause rare patient adverse events.
The recall record does not specify a remedy, so no action is required beyond checking if your device is affected.
Check for model numbers 1101210000, 1101210100, or 1101210200 and production dates from April 1, 2025 to August 20, 2025.
We’ve drafted a message you can send Lutronic to request your refund or repair — edit it as you like.
Subject: Recall Z-0146-2026 — Lutronic Lutronic Hello, I own a Lutronic that is covered by recall Z-0146-2026 from Lutronic. 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.
