CONDUIT CET30131TRecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10705034555713), received between Jun 26, 2024 and Mar 2, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Contamination /Decontamination 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. How this data works · Data updated Oct 13, 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.

• MalfunctionMar 2, 2026Material Deformation

  IT WAS REPORTED THAT THE SLENDER INSERTER WAS FOUND BENT AT THE FRONT, SPECIFICALLY THE PART IN CONTACT WITH BONE, DURING SURGERY WHEN AN IMPLANT WAS INSERTED. THE BENDING WAS SUSPECTED TO HAVE OCCURRED DURING A PREVIOUS SURGERY AND WAS ATTRIBUTED TO A POSSIBLE DESIGN CHALLENGE, AS THE INNER PART WITH A STOP CAN DEFORM WHEN MEETING BONE FROM THE VERTEBRAL BODY ABOVE OR BELOW THE DISC. THERE WAS NO REPORTED PATIENT HARM OR SIGNIFICANT DELAY ASSOCIATED WITH THE EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24482014 ↗
• MalfunctionNov 18, 2025Corroded; Contamination /Decontamination Problem; No Apparent Adverse Event; Illegible Information; Corroded; Contamination /Decontamination Problem; No Apparent Adverse Event; Illegible Information

  IT WAS REPORTED THAT DURING CLEANING PROCESS IT WAS IDENTIFIED THAT THE TEXT ON THE INSTRUMENTS START TO FADE AND THERE WAS FINE SIGNS OF RUST ON INSTRUMENTS WHEN CLEANING AFTER A SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23586687 ↗
• MalfunctionNov 18, 2025Corroded; Contamination /Decontamination Problem; Illegible Information; Corroded; Contamination /Decontamination Problem; Illegible Information

  IT WAS REPORTED THAT DURING CLEANING PROCESS IT WAS IDENTIFIED THAT THE TEXT ON THE INSTRUMENTS START TO FADE AND THERE WAS FINE SIGNS OF RUST ON INSTRUMENTS WHEN CLEANING AFTER A SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23586670 ↗
• MalfunctionJun 26, 2024Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED DURING A LEVEL 2 ACDF PROCEDURE ON (B)(6) 2024, THE SLENDER INSERTER TEETH DO NOT OPEN WIDE ENOUGH TO GRAB THE IMPLANT CAGE. INSTEAD, THE SCRUB HAD TO LATCH ONE TOOTH OF THE INSERTER INTO THE IMPLANT AND THEN LEVERAGE THE OTHER TOOTH AND AN AUDIBLE CLICK WAS HEARD AS IT SNATCHED THE IMPLANT. THERE WAS NO PATIENT COMPLICATIONS, THE CASE WAS COMPLETED SUCCESSFULLY. THIS REPORT IS FOR ONE SLENDER INSERTER THIS IS REPORT 1 OF 1 FOR (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19613983 ↗