n.a. 37270DLRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04048551155530), received between Nov 12, 2025 and Nov 12, 2025 — classified as 2 injuries.

The most frequently reported specific device problem is “Break” (2 reports).

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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryNov 12, 2025Break; Break

  IT WAS REPORTED THAT THE SURGEON WAS USING THE ELECTRODE PROBE TO PUSH DOWN THE FIBROID. IT WAS THEN THE SURGEON REALIZED THAT THE TIP OF THE INSTRUMENT WAS MISSING. IT WAS AGREED UPON TO SHOOT X-RAY TO DETERMINE WHETHER THE TIP WAS LEFT INSIDE THE PATIENT OR DROPPED OUT. AFTER X-RAY, IT WAS FOUND THAT TIP WAS LEFT INSIDE THE PATIENT. THE PATIENT HAD TO UNDERGO REMOVAL OF THE TIP.

  Patient problems: Insufficient Information; Unintended Radiation Exposure

  MAUDE report 23534502 ↗
• InjuryNov 12, 2025Break; Break

  IT WAS REPORTED THAT THE SURGEON WAS USING THE ELECTRODE PROBE TO PUSH DOWN THE FIBROID. IT WAS THEN THE SURGEON REALIZED THAT THE TIP OF THE INSTRUMENT WAS MISSING. IT WAS AGREED UPON TO SHOOT X-RAY TO DETERMINE WHETHER THE TIP WAS LEFT INSIDE THE PATIENT OR DROPPED OUT. AFTER X-RAY, IT WAS FOUND THAT TIP WAS LEFT INSIDE THE PATIENT. THE PATIENT HAD TO UNDERGO REMOVAL OF THE TIP.

  Patient problems: Insufficient Information; Unintended Radiation Exposure

  MAUDE report 23534355 ↗