EXPEDIUM VERSE 199721870Recalls & reported problems
Medos International Sàrl · EXPEDIUM VERSE SPINE SYSTEM POLYAXIAL SCREW 5.5 8.0 x 70mm · Class 2 · Implant
All models of EXPEDIUM VERSE (90)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705034441900), received between Jul 13, 2022 and Jul 13, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Twisted/Bent” (1 report).
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.
Most reported problems
Device problems
- Material Twisted/Bent1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 13, 2022Material Twisted/Bent; Material Twisted/Bent
DEVICE REPORT FROM GERMANY REPORTS AN EVENT AS FOLLOWS: IT WAS REPORTED THAT DURING A PROCEDURE ON (B)(6) 2022, THE SURGEON HAD PLACED ALL SCREWS, INSERTED A TI ROD AND COCR ROD, AND BEGAN INSERTION OF THE CORRECTION CLOSER SCREWS FROM THE CAUDAL SIDE. ON THE SIDE WITH THE COCR ROD, THE CORRECTION SCREW PLUGS JUMPED IN THE THREAD ON THE 2ND EXP VERSE SCREW, DAMAGING THE THREAD IN THE TULIP OF THE SCREW. THE SAME EVENT OCCURRED WITH THE 4TH SCREW, BOTH SCREWS REQUIRED REPLACEMENT. THE ROD HAD TO BE REMOVED IN ORDER TO REPLACE THE SCREWS. AFTER THIS EVENT, THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH REPLACEMENT PRODUCTS. THERE WAS A SURGICAL DELAY OF 30-40 MINUTES. PATIENT OUTCOME IS STABLE. THIS REPORT IS FOR A EXPEDIUM VERSE SPINE SYSTEM POLYAXIAL SCREW 5.5 8.0 X 70MM. THIS IS REPORT 1 OF 6 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15004569 ↗
Other Orthosis, spondylolisthesis spinal fixation devices
- CD HORIZON® Spinal System 7540020Medtronic Sofamor Danek, Inc. · Orthosis, spondylolisthesis spinal fixation257 reports
- MANTIS Redux 48289999Stryker Corporation · Orthosis, spondylolisthesis spinal fixation76 reports
- EXPEDIUM TOP NOTCH 179771555Depuy Spine, LLC · Orthosis, spondylolisthesis spinal fixation41 reports
- EXPEDIUM 179712650Medos International Sàrl · Orthosis, spondylolisthesis spinal fixation31 reports
- EXPEDIUM VERSE 199721530Medos International Sàrl · Orthosis, spondylolisthesis spinal fixation29 reports
- XIA 4 5 48130000Stryker Corporation · Orthosis, spondylolisthesis spinal fixation29 reports
- XIA 4.5 System - XIA CT 48850000Stryker Corporation · Orthosis, spondylolisthesis spinal fixation27 reports
- CD HORIZON® Spinal System 7576545Medtronic Sofamor Danek, Inc. · Orthosis, spondylolisthesis spinal fixation26 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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