EXPEDIUM 279702700NRecalls & reported problems
Medos International Sàrl · UNIVERSAL NAVIGATION EXPEDIUM SPINE SYSTEM TAP, DUAL LEAD 7mm · Class 2
All models of EXPEDIUM (291)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 10
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI 10705034388373), received between Sep 12, 2024 and Dec 12, 2025 — classified as 10 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (5 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Cut5
- Material Deformation5
Patient problems
- No Clinical Signs, Symptoms or Conditions10
Recent adverse event reports
The 10 most recent of 10 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 12, 2025Material Deformation; Material Deformation
IT WAS REPORTED ON AN UNKNOWN DATE THAT TAP INSTRUMENT IS BENT DUE TO USE. NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23789711 ↗MalfunctionDec 12, 2025Material Deformation; Material Deformation
IT WAS REPORTED ON AN UNKNOWN DATE THAT TAP INSTRUMENT IS BENT DUE TO USE. NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23789660 ↗MalfunctionDec 12, 2025Material Deformation; Material Deformation
IT WAS REPORTED ON AN UNKNOWN DATE THAT TAP INSTRUMENT IS BENT DUE TO USE. NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23789657 ↗MalfunctionDec 12, 2025Material Deformation; Material Deformation
IT WAS REPORTED ON AN UNKNOWN DATE THAT TAP INSTRUMENT IS BENT DUE TO USE. NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23789647 ↗MalfunctionDec 12, 2025Material Deformation; Material Deformation
IT WAS REPORTED ON AN UNKNOWN DATE THAT TAP INSTRUMENT IS BENT DUE TO USE. NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23789635 ↗MalfunctionSep 12, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED THAT ON AN UNKNOWN DATE IN 2024, THE TAPS WERE DULL, UNABLE TO BE USED. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20203192 ↗MalfunctionSep 12, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED THAT ON AN UNKNOWN DATE IN 2024, THE TAPS WERE DULL, UNABLE TO BE USED. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20203027 ↗MalfunctionSep 12, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED THAT ON AN UNKNOWN DATE IN 2024, THE TAPS WERE DULL, UNABLE TO BE USED. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20203005 ↗MalfunctionSep 12, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED THAT ON AN UNKNOWN DATE IN 2024, THE TAPS WERE DULL, UNABLE TO BE USED. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20202927 ↗MalfunctionSep 12, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED THAT ON AN UNKNOWN DATE IN 2024, THE TAPS WERE DULL, UNABLE TO BE USED. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20201525 ↗
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- VELYS 4515-70-106Depuy (Ireland) · Orthopedic stereotaxic instrument564 reports
- NA 209999Mako Surgical Corp. · Orthopedic stereotaxic instrument522 reports
- Mazor X System TPL0059-06Mazor Robotics Ltd · Orthopedic Stereotaxic Instrument2 recalls2 deaths392 reports
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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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