CONDUIT TFT20102TRecalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 10705034557496), received between Mar 8, 2023 and May 29, 2026 — classified as 1 injury, 7 malfunctions.

The most frequently reported specific device problem is “Device-Device Incompatibility” (7 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 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 29, 2026Device-Device Incompatibility

  IT WAS REPORTED THE KNOB AND INNERSHAFT IS STUCK IN/ON THE OUTER SHAFT. IT WAS NOT POSSIBLE TO DISASSEMBLE THE 3 PARTS. NO CONSEQUENCE FOR PATIENT. SURGERY PERFORMED AS PLANNED. ANOTHER INSTRUMENT WAS USED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25330270 ↗
• MalfunctionFeb 5, 2026Mechanical Jam

  IT WAS REPORTED THAT THE CONDUIT TRIAL INSERTER COULDN'T BE DISASSEMBLED ANYMORE. THE KNOB WAS STUCK ON THE OUTER SHAFT, AND THE INNER SHAFT WAS ALSO STUCK WITHIN THE OUTER SHAFT. THERE WAS NO PATIENT CONSEQUENCE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24269346 ↗
• MalfunctionAug 4, 2025Corroded; Device-Device Incompatibility; Corroded; Device-Device Incompatibility

  IT WAS REPORTED THAT THE INSERTER PRODUCTS ARE WORN DUE TO FREQUENT USE AND NEED REPLACEMENT. THE HAMMER BROKE AND HAS A CRACK LINE. THE INSERTER KNOB HAS CORRODED THREADS AND IT IS NOT POSSIBLE TO FIT INTO THE OUTER SHAFT. THE TRIAL IS THE OLD REFERENCE SO IT DOESN¿T ALLOW CONNECTION WITH THE NEW OUTER AND INNER SHAFTS. ANOTHER TRIAL WAS WORN OUT AND ROTATED RELATIVE TO THE OUTER SHAFT WHILE IT WAS COMPLETELY CLOSED. THERE WAS NO PATIENT CONSEQUENCE. ISSUES WERE NOTED PREOPERATIVELY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22700954 ↗
• MalfunctionJun 2, 2025Break; Device-Device Incompatibility; Break; Device-Device Incompatibility

  ADDITIONAL INFORMATION RECEIVED STATES THAT ON 06/26/2025, IT WAS DISCOVERED THAT THE DEVICE (TFT30101T; NN180321) WAS DEFORMED AND STRIPPED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22123522 ↗
• MalfunctionJan 2, 2025Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED DURING A SPINAL FUSION PROCEDURE ON (B)(6) 2024, THE CONDUIT TLIF INSERTER CANNOT BE DISMANTLED. THE PROCEDURE WAS COMPLETED WITH NO CONSEQUENCES TO THE PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21055259 ↗
• MalfunctionNov 12, 2024Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT THIS WAS AN UNKNOWN SURGERY PERFORMED ON (B)(6) 2024. THE INSERTER KNOB AND THE TRIAL INSERTER INNER SHAFT BECAME UNABLE TO BE DETACHED. THE SURGERY WAS COMPLETED SUCCESSFULLY WITHOUT ANY SURGICAL DELAY. NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20667092 ↗
• InjuryMay 20, 2024Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A SPINAL FUSION SURGERY ON (B)(6) 2024 FOR A SINGLE-SEGMENTAL MIS TLIF TREATMENT. THE PRE-PREPARED INTERVERTEBRAL DISC SPACE L4-L5 WAS PREPARED WITH AN INTERVERTEBRAL DISC KNIFE TO A HEIGHT OF 11MM. THE INSTRUMENT TECHNICIAN THEN CORRECTLY ASSEMBLED THE CONDUIT IMPLANT HOLDER AND CONNECTED IT TO A CONDUIT TLIF CAGE 9MM/10X28/8°. IT WAS ENSURED THAT THE ROTARY KNOB OF THE IMPLANT HOLDER WAS TURNED CLOCKWISE AS TIGHTLY AS POSSIBLE. THE DOCTOR PLACED THE IMPLANT AT THE ENTRANCE TO THE INTERVERTEBRAL DISC SPACE AND HIT THE IMPLANT KNOB OF THE IMPLANT HOLDER WITH THE HAMMER. THE CONDUIT TLIF CAGE ONLY PENETRATED THE INTERVERTEBRAL DISC SPACE WITH THE "BULLET NOSE" BEFORE THE RIGID CONNECTION BETWEEN THE CAGE AND THE IMPLANT HOLDER BECAME LOOSE AND THE IMPLANT HOLDER SWIVELED 90° INTO THE SPINAL CANAL IN AN UNPLANNED MANNER. DR REMOVED THE IMPLANT HOLDER WITH CAGE WITH A KNOCK-OUT HAMMER AND HAD THE CAGE CONNECTED FROM THE INSTRUMENT ATRINE TO ANOTHER IDENTICAL IMPLANT HOLDER. WITH THIS "NEW" IMPLANT HOLDER, INSERTING THE SAME CONDUIT CAGE WAS POSSIBLE WITHOUT ANY PROBLEMS. WHEN THE CAGE WAS FLIPPED THREE TIMES EARLY, A SENSITIVE ROOT INJURY OCC

  Patient problems: Nerve Damage

  MAUDE report 19352771 ↗
• MalfunctionMar 8, 2023Device-Device Incompatibility; Device-Device Incompatibility

  THE SURGERY WAS COMPLETED SUCCESSFULLY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16504396 ↗