EXPEDIUM 299704105Recalls & reported problems
Medos International Sàrl · EXPEDIUM SPINE SYSTEM THORACIC PEDICLE PROBE, STRAIGHT 10-60mm Plus or Minus 2 Percent · Class 1
All models of EXPEDIUM (291)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10705034467351), received between Jan 25, 2023 and Oct 27, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Break” (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.
Reports received per month
Most reported problems
Device problems
- Break3
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 27, 2025Break; Break
IT WAS REPORTED THAT THE DEVICE WAS DAMAGED/BROKEN. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23389175 ↗MalfunctionFeb 1, 2023Break; Break
IT WAS REPORTED ON (B)(6) 2023, PEDICLE FINDER TIP BROKE OFF IN PATIENT DURING X-RAY. THEY HAD TO OPEN REMOVAL REVERSE THREAD TO REMOVE BROKEN PEDICLE FINDER. THE SURGERY WAS COMPLETED SUCCESSFULLY WITH A SURGICAL DELAY OF 5 MINUTES. THERE WERE NO PATIENT OUTCOMES REPORTED. THERE WERE NO FRAGMENTS GENERATED. THIS REPORT IS FOR ONE (1) THORACIC PEDICLE PROBE, ST. THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16277586 ↗MalfunctionJan 25, 2023Break; Break
DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN UNITED KINGDOM AS FOLLOWS: IT WAS REPORTED ON (B)(6) 2023, THAT THE SURGEON WAS USING THE FINDER WHEN THE TIP SNAPPED OFF. ANOTHER SET IN THE HOSPITAL WAS USED. THERE WAS NO SURGICAL DELAY. THIS REPORT IS FOR ONE (1) THORACIC PEDICLE PROBE, ST. THIS IS REPORT 1 OF 1 FOR COMPLAINT: (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16242130 ↗
Other PROBE devices
- EXPEDIUM 279702030Depuy Spine, LLC · PROBE53 reports
- Sklar 96-2361Sklar Corporation · PROBE1 recall0 reports
- Sklar Instruments 94-5923Sklar Corporation · PROBE1 recall0 reports
- MOSS 275010140Depuy Spine, LLC · PROBE28 reports
- EXPEDIUM 279702040Depuy Spine, LLC · PROBE21 reports
- MULTILOC 03.019.029Synthes GmbH · PROBE15 reports
- MOSS 275010160Depuy Spine, LLC · PROBE11 reports
- EXPEDIUM 279702010Depuy Spine, LLC · PROBE9 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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