CONDUITRecalls & reported problems across all models
Medos International Sàrl · 27 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 187
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls
- 0
We found 27 models of CONDUIT by Medos International Sàrl in the FDA's device registry (GUDID). Together they are named in 187 adverse event reports in the FDA's MAUDE database, received between Apr 14, 2022 and Sep 29, 2026 — classified as 4 injuries, 183 malfunctions.
The most frequently reported specific device problem is “Device-Device Incompatibility” (131 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported CONDUIT problems
Device problems
- Device-Device Incompatibility131
- Material Deformation29
- Material Twisted/Bent18
- Break15
- Mechanical Jam9
- Appropriate Device Problem Term/Code Not Available7
- Contamination /Decontamination Problem6
- Material Integrity Problem4
Patient problems
- No Clinical Signs, Symptoms or Conditions169
- Insufficient Information12
- Nerve Damage3
- Hemorrhage/Blood Loss/Bleeding2
- Perforation of Vessels1
CONDUIT models
27 models, most reported first. Each model has its own page with its reports, recalls and device details.
- CONDUIT TFT20101TIntervertebral fusion device with bone graft, lumbar48 reports
- CONDUIT TFT30102TIntervertebral fusion device with bone graft, lumbar22 reports
- CONDUIT TFT30101TIntervertebral fusion device with bone graft, lumbar20 reports
- CONDUIT PET30102TIntervertebral fusion device with bone graft, lumbar19 reports
- CONDUIT TFT20103TIntervertebral fusion device with bone graft, lumbar13 reports
- CONDUIT PET30101TIntervertebral fusion device with bone graft, lumbar12 reports
- CONDUIT TFT20102TIntervertebral fusion device with bone graft, lumbar8 reports
- CONDUIT 187210110Intervertebral fusion device with bone graft, lumbar8 reports
- CONDUIT LET20100TIntervertebral fusion device with bone graft, lumbar7 reports
- CONDUIT CET30131TIntervertebral fusion device with bone graft, cervical4 reports
- CONDUIT LET20101TIntervertebral fusion device with bone graft, lumbar4 reports
- CONDUIT LET30101TIntervertebral fusion device with bone graft, lumbar2 reports
- CONDUIT PET10710TRETRACTOR2 reports
- CONDUIT PFT10700TOrthopedic manual surgical instrument2 reports
- CONDUIT PFT10800TOrthopedic manual surgical instrument2 reports
- CONDUIT 187210120Intervertebral fusion device with bone graft, lumbar2 reports
- CONDUIT 187210210Intervertebral fusion device with bone graft, lumbar2 reports
- CONDUIT AET10210TIntervertebral fusion device with bone graft, lumbar1 report
- CONDUIT AET10208TIntervertebral fusion device with bone graft, lumbar1 report
- CONDUIT CET30101TIntervertebral fusion device with bone graft, cervical1 report
- CONDUIT LET30100TIntervertebral fusion device with bone graft, lumbar1 report
- CONDUIT LET30200TIntervertebral fusion device with bone graft, lumbar1 report
- CONDUIT TFT80932TIntervertebral fusion device with bone graft, lumbar1 report
- CONDUIT PET21010TIntervertebral fusion device with bone graft, lumbar1 report
- CONDUIT PET20910TIntervertebral fusion device with bone graft, lumbar1 report
- CONDUIT PET30200TIntervertebral fusion device with bone graft, lumbar1 report
- CONDUIT 187210310Intervertebral fusion device with bone graft, lumbar1 report
Recent CONDUIT adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Contamination /Decontamination Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50936458 ↗MalfunctionSep 29, 2026Device-Device Incompatibility; Material Deformation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50934906 ↗MalfunctionSep 29, 2026Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50934905 ↗MalfunctionSep 29, 2026Device-Device Incompatibility; Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50932549 ↗MalfunctionSep 24, 2026Device-Device Incompatibility; Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50892352 ↗MalfunctionSep 23, 2026Material Deformation
It was reported that the inner shaft got tilted while hammering the cage. There was no patient harm and no surgical delay reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50871537 ↗MalfunctionSep 15, 2026Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50777091 ↗MalfunctionSep 15, 2026Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50777088 ↗MalfunctionSep 15, 2026Material Deformation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50775731 ↗MalfunctionSep 9, 2026Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50698641 ↗MalfunctionJul 27, 2026Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50007774 ↗MalfunctionJul 16, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25841192 ↗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 25330342 ↗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 ↗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 25330156 ↗
Other Medos International Sàrl products
- TRUESPAN ORTHOCORD6 models · 4,109 reports
- FMS39 models · 3,588 reports
- EXPEDIUM291 models · 3,312 reports
- EXPEDIUM VERSE90 models · 2,686 reports
- EXPRESSEW6 models · 2,459 reports
- OMNISPAN ORTHOCORD3 models · 1,581 reports
- HEALIX ADVANCE ORTHOCORD21 models · 1,311 reports
- PROWLER SELECT9 models · 1,066 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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