Codman 901001IRRORecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10886704081692), received between Mar 8, 2022 and Aug 22, 2022 — classified as 2 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 16, 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.

• MalfunctionAug 22, 2022Electrical /Electronic Property Problem; Electrical /Electronic Property Problem

  A FACILITY REPORTED THE FUSES OF A ELECTROSURGICAL IRRIGATOR BLOW WITH EVERY USE. PRODUCT WAS IN CONTACT WITH THE PATIENT, NO PATIENT INJURY REPORTED; HOWEVER, THERE WAS APPROXIMATELY 30 MINUTES SURGICAL DELAY DUE TO IRRIGATOR FAILURE. THE PROCEDURE WAS COMPLETED WITH A REPLACEMENT PRODUCT AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15267896 ↗
• MalfunctionMar 8, 2022Electrical /Electronic Property Problem; Electrical /Electronic Property Problem

  A FACILITY REPORTED AN ELECTROSURGICAL IRRIGATOR WITH A DEFECTIVE FUSE. PRODUCT WAS IN CONTACT WITH THE PATIENT; HOWEVER, NO PATIENT INJURY WAS REPORTED AND THE EVENT LED TO 30 MINUTES SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13694670 ↗