CONDUIT PET10710TRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10705034557144), received between Sep 17, 2024 and Mar 30, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Device-Device Incompatibility” (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.

• MalfunctionMar 30, 2026Device-Device Incompatibility

  IT WAS REPORTED THAT THE HANDLE CRACKED AND BROKE WHEN LIGHT MALLETING WAS REQUIRED FOR EXTRACTION FROM THE DISC SPACE. ON REMOVING THE INSTRUMENT, HANDLE AND DISTRACTOR, THE 7MM DISTRACTOR WAS OBSERVED TO BE JAMMED IN THE HANDLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24718568 ↗
• MalfunctionSep 17, 2024Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED DURING A PROCEDURE ON AN UNKNOWN DATE IN 2024, ONE DISTRACTOR AND 2 SHAVERS COULDN¿T BE TAKEN AWAY FROM THEIR HANDLE. NO IMPACT ON SURGERY, NO IMPACT ON PATIENT. NO SURGICAL DELAY. PROCEDURE WAS COMPLETED SUCCESSFULLY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20241585 ↗