n.a. 27050GP-SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04048551395592), received between Jan 8, 2026 and Jan 8, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).

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 16, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionJan 8, 2026Detachment of Device or Device Component

  THE EVENT OCCURRED IN CANADA ACCORDING TO THE INFORMATION RECEIVED, ELECTRODE BROKE AT THE END OF THE CASE. THEY CHANGED THE ELECTRODE AND FINISHED THE CASE. AFTER THE SET WAS CLEANED IN MDRD, IT WAS NOTED THAT THE SCOPE HAD BEEN DAMAGED. NO INJURY TO PATIENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24003304 ↗