MEDLINE RENEWAL 279401200RHRecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10888277700659), received between May 22, 2026 and Sep 28, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 28, 2026Electrical /Electronic Property Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50923295 ↗
• MalfunctionSep 19, 2026Corroded; Device Remains Activated

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50831818 ↗
• MalfunctionJun 11, 2026Communication or Transmission Problem

  IT WAS REPORTED THAT, PLUGGED DEVICE IN AND IT WOULD NOT CONNECT OR REGISTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25480796 ↗
• MalfunctionMay 22, 2026Electrical /Electronic Property Problem

  IT WAS REPORTED THAT, WHEN STAFF PLUGGED IN THE SERFA WAND, THE GENERATOR SAID NOT RECOGNIZED. CORD WAS MOVED TO DIFFERENT POSITIONS WHICH ALLOWED THE DEVICE TO WORK AND THEN QUICKLY DISCONNECT SAYING DISCONNECTED. IT SEEMED LIKE AN ELECTRICAL SHORT IN THE CORD. THE STAFF GRABBED A NEW DEVICE AND FINISHED THE CASE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25251037 ↗