CONDUIT LET20100TRecalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10705034557069), received between Mar 27, 2023 and Oct 22, 2025 — classified as 7 malfunctions.

The most frequently reported specific device problem is “Device-Device Incompatibility” (3 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 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 22, 2025Device-Device Incompatibility; Material Deformation; Device-Device Incompatibility; Material Deformation

  IT WAS REPORTED THAT DURING A PROCEDURE, THE INSTRUMENT FOR INSERTING THE TRIALS HAS THREADS AFFECTED BY NUMEROUS IMPACTS OF THE HAMMER AND THE THREADS HAVE BEEN AFFECTED AND MAY HAVE CAUSED A DENT DUE TO IT. IT IS NOW HARD TO ATTACH THE INSTRUMENTS TOGETHER. SURGICAL TEAM MADE DO WITH WHAT WAS PROVIDED IN THE SET. THERE WAS NO PATIENT CONSEQUENCE. THERE WAS A SURGICAL DELAY OF A COUPLE OF MINUTES.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23359416 ↗
• MalfunctionJul 15, 2024Device-Device Incompatibility; Material Twisted/Bent; Device-Device Incompatibility; Material Twisted/Bent

  IT WAS REPORTED THAT ON JUNE 11, 2024 AFTER INSTRUMENTS WENT THROUGH STERILE TO BE CLEANED, THE INSTRUMENT WOULD NOT COME APART. THE END LOCKING KNOB IS CROSS THREADED AND WOULD NOT MOVE. THERE WAS NO PATIENT INVOLVEMENT. THIS REPORT INVOLVES ONE (1) CONDUIT LATERAL LUMBAR INTERBODY TRIAL INSERTER OUTER SHAFT. THIS IS REPORT 1 OF 1 FOR (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19741692 ↗
• MalfunctionJul 12, 2024Mechanical Jam; Mechanical Jam

  IT WAS REPORTED THAT ON (B)(6) 2024, POST-OPERATIVELY THE INNER SHAFT OF THE CONDUIT LLIF TRIAL IMPLANT IS STUCK AND CAN NO LONGER BE REMOVED. THERE WAS NO PATIENT CONSEQUENCE. THIS REPORT IS FOR ONE (1) TRIAL INSERTER OUTER SHAFT. THIS IS REPORT 1 OF 4 FOR (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19733930 ↗
• MalfunctionJul 12, 2024Mechanical Jam; Mechanical Jam

  IT WAS REPORTED THAT ON (B)(6) 2024, POST-OPERATIVELY THE INNER SHAFT OF THE CONDUIT LLIF TRIAL IMPLANT IS STUCK AND CAN NO LONGER BE REMOVED. THERE WAS NO PATIENT CONSEQUENCE. THIS REPORT IS FOR ONE (1) TRIAL INSERTER OUTER SHAFT THIS IS REPORT 3 OF 4 FOR (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19733889 ↗
• MalfunctionDec 8, 2023Device-Device Incompatibility; Device-Device Incompatibility

  NO OTHER MEDICAL INTERVENTION WAS REQUIRED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18291232 ↗
• MalfunctionMar 27, 2023Material Deformation; Material Deformation

  IT WAS REPORTED THAT ON (B)(6) 2023, SALES REPRESENTATIVE HAVE BEEN INFORMED BY MARKETING TO FILE THE BELOW COMPLAINT. THE SALES REPRESENTATIVE NOTICED THAT THE TIPS OF THE CONDUIT LATERAL TRIAL INSERTER ARE BECOMING DEFORMED WITH USE. THIS IS CAUSING THE BALL TIP ON THE INNER SHAFT TO NOT EASILY PASS THROUGH THE TIP OF THE OUTER INSERTER SHAFT. THIS DEFORMATION HAS PROGRESSED TO THE POINT WHERE DURING ASSEMBLY A MALLET IS USED TO TAP THE INNER BALL TIPPED SHAFT PASSED THE TIP OF THE INSERTER WHERE IT INTERFACES WITH THE TRIAL. TO DISASSEMBLE AND REMOVE THE INNER SHAFT FROM THE TRIAL INSERTER SALES REPRESENTATIVE USING A SLAP HAMMER ATTACHED TO THE INSERTER KNOB TO FORCE THE BALL TIP PAST THE DEFORMED TIP. THIS IS HAPPENING WITH 2 OF THE CONDUIT LATERAL TRIAL INSERTERS. IT SEEMS TO BE PROGRESSING OVER TIME AND USAGE. ALSO, THE SALES CONSULTANT NOTICING DEFORMATION OF CONDUIT LATERAL TRIAL INSERTER IS DEFORMING FROM REPEATED USAGE. IT IS AFFECTING ASSEMBLY AND DISASSEMBLY OF THE INSERTER BUT NOT THE FUNCTION. THE ISSUE APPEARS TO BE RELATED TO GENERAL USAGE AND NOT ONE SPECIFIC EVENT. THIS COMPLAINT INVOLVES ONE (1) DEVICE. THIS REPORT IS FOR ONE (1) TRIAL INSERTER OUTER SHAFT THIS

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16622508 ↗
• MalfunctionMar 27, 2023Material Deformation; Material Deformation

  IT WAS REPORTED THAT ON MARCH 8, 2023, SALES REPRESENTATIVE HAVE BEEN INFORMED BY MARKETING TO FILE THE BELOW COMPLAINT. THE SALES REPRESENTATIVE NOTICED THAT THE TIPS OF THE CONDUIT LATERAL TRIAL INSERTER ARE BECOMING DEFORMED WITH USE. THIS IS CAUSING THE BALL TIP ON THE INNER SHAFT TO NOT EASILY PASS THROUGH THE TIP OF THE OUTER INSERTER SHAFT. THIS DEFORMATION HAS PROGRESSED TO THE POINT WHERE DURING ASSEMBLY A MALLET IS USED TO TAP THE INNER BALL TIPPED SHAFT PASSED THE TIP OF THE INSERTER WHERE IT INTERFACES WITH THE TRIAL. TO DISASSEMBLE AND REMOVE THE INNER SHAFT FROM THE TRIAL INSERTER SALES REPRESENTATIVE USING A SLAP HAMMER ATTACHED TO THE INSERTER KNOB TO FORCE THE BALL TIP PAST THE DEFORMED TIP. THIS IS HAPPENING WITH 2 OF THE CONDUIT LATERAL TRIAL INSERTERS. IT SEEMS TO BE PROGRESSING OVER TIME AND USAGE. ALSO, THE SALES CONSULTANT NOTICING DEFORMATION OF CONDUIT LATERAL TRIAL INSERTER IS DEFORMING FROM REPEATED USAGE. IT IS AFFECTING ASSEMBLY AND DISASSEMBLY OF THE INSERTER BUT NOT THE FUNCTION. THE ISSUE APPEARS TO BE RELATED TO GENERAL USAGE AND NOT ONE SPECIFIC EVENT. THIS COMPLAINT INVOLVES ONE (1) DEVICE. THIS REPORT IS FOR ONE (1) TRIAL INSERTER OUTER SHAFT. TH

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16622506 ↗