CONDUIT LET20101TRecalls & reported problems
Medos International Sàrl · CONDUIT Lateral Lumbar Interbody Trial Inserter Inner Shaft · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10705034557052), received between May 7, 2024 and Nov 12, 2024 — classified as 4 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.
Reports received per month
Most reported problems
Device problems
- Device-Device Incompatibility2
- Mechanical Jam2
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
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 20665911 ↗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 INNER SHAFT. THIS IS REPORT 4 OF 4 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19733940 ↗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 INNER SHAFT THIS IS REPORT 2 OF 4 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19733721 ↗MalfunctionMay 7, 2024Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT AFTER A PROCEDURE ON (B)(6) 2024, THE TRIAL INSERTER INNER SHAFT COULD NOT BE REMOVED FROM THE TRIAL INSERTER OUTER SHAFT. IT WAS NOTED THERE WAS NO IMPACT ON THE PATIENT OR PROCEDURE. THIS REPORT IS FOR A TRIAL INSERTER INNER SHAFT. THIS IS REPORT 2 OF 2 FOR (B)(4) .
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19259786 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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