EXPEDIUM VERSERecalls & reported problems across all models
Medos International Sàrl · 90 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2,686
- Deaths reported
- 3
- Injuries reported
- 868
- Recalls
- 0
We found 90 models of EXPEDIUM VERSE by Medos International Sàrl in the FDA's device registry (GUDID). Together they are named in 2,686 adverse event reports in the FDA's MAUDE database, received between Aug 3, 2017 and Sep 25, 2026 — classified as 3 deaths, 868 injuries, 1,815 malfunctions.
The most frequently reported specific device problem is “Material Twisted/Bent” (1,065 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 EXPEDIUM VERSE problems
Device problems
- Material Twisted/Bent1,065
- Adverse Event Without Identified Device or Use Problem447
- Break391
- Device-Device Incompatibility383
- Device Slipped100
- Loose or Intermittent Connection99
- Material Deformation81
- Migration62
Patient problems
- No Clinical Signs, Symptoms or Conditions1,501
- Unspecified Infection293
- No Consequences Or Impact To Patient288
- No Code Available156
- Failure of Implant102
- Insufficient Information86
- Not Applicable78
- Neurological Deficit/Dysfunction58
EXPEDIUM VERSE models
90 models, most reported first. Each model has its own page with its reports, recalls and device details.
- EXPEDIUM VERSE 299704230DRIVER, PROSTHESIS875 reports
- EXPEDIUM VERSE 199721000Orthosis, spinal pedicle fixation, for degenerative disc disease387 reports
- EXPEDIUM VERSE 199721001APPLIANCE, FIXATION, SPINAL INTERLAMINAL227 reports
- EXPEDIUM VERSE 299704155DRIVER, PROSTHESIS151 reports
- EXPEDIUM VERSE 199721001SThoracolumbosacral pedicle screw system124 reports
- EXPEDIUM VERSE 199721000SThoracolumbosacral pedicle screw system97 reports
- EXPEDIUM VERSE 299704152ORTHOPEDIC MANUAL SURGICAL INSTRUMENT84 reports
- EXPEDIUM VERSE 299704220DRIVER, PROSTHESIS56 reports
- EXPEDIUM VERSE 199721535Orthosis, spinal pedicle fixation, for degenerative disc disease46 reports
- EXPEDIUM VERSE 299704217ORTHOPEDIC MANUAL SURGICAL INSTRUMENT42 reports
- EXPEDIUM VERSE 199721640ORTHOSIS, SPINAL PEDICLE FIXATION35 reports
- EXPEDIUM VERSE 299704215ORTHOPEDIC MANUAL SURGICAL INSTRUMENT32 reports
- EXPEDIUM VERSE 199721530Orthosis, spondylolisthesis spinal fixation29 reports
- EXPEDIUM VERSE 199723645SThoracolumbosacral pedicle screw system2 deaths29 reports
- EXPEDIUM VERSE 199723650ORTHOSIS, SPINAL PEDICLE FIXATION27 reports
- EXPEDIUM VERSE 199721645Orthosis, spinal pedicle fixation, for degenerative disc disease1 death27 reports
- EXPEDIUM VERSE 299704160ORTHOPEDIC MANUAL SURGICAL INSTRUMENT26 reports
- EXPEDIUM VERSE 199721540Orthosis, spondylolisthesis spinal fixation24 reports
- EXPEDIUM VERSE 199723745SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL24 reports
- EXPEDIUM VERSE 199723640SThoracolumbosacral pedicle screw system22 reports
- EXPEDIUM VERSE 199723645bone cement, posterior screw augmentation21 reports
- EXPEDIUM VERSE 3010-19-008Orthopedic stereotaxic instrument21 reports
- EXPEDIUM VERSE 199723745bone cement, posterior screw augmentation13 reports
- EXPEDIUM VERSE 199721745APPLIANCE, FIXATION, SPINAL INTERLAMINAL13 reports
- EXPEDIUM VERSE 199721635Orthosis, spondylolisthesis spinal fixation13 reports
- EXPEDIUM VERSE 199723750SThoracolumbosacral pedicle screw system13 reports
- EXPEDIUM VERSE 199723750ORTHOSIS, SPINAL PEDICLE FIXATION12 reports
- EXPEDIUM VERSE 199723740SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL12 reports
- EXPEDIUM VERSE 3010-19-041Orthopedic stereotaxic instrument12 reports
- EXPEDIUM VERSE 199723640ORTHOSIS, SPINAL PEDICLE FIXATION11 reports
- EXPEDIUM VERSE 199721650Pedicle screw spinal system, adolescent idiopathic scoliosis10 reports
- EXPEDIUM VERSE 199723650SAppliance, fixation, spinal intervertebral body10 reports
- EXPEDIUM VERSE 199723545ORTHOSIS, SPINAL PEDICLE FIXATION9 reports
- EXPEDIUM VERSE 199723655SThoracolumbosacral pedicle screw system8 reports
- EXPEDIUM VERSE 199721750ORTHOSIS, SPINAL PEDICLE FIXATION7 reports
- EXPEDIUM VERSE 199723545SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL7 reports
- EXPEDIUM VERSE 299704285ORTHOPEDIC MANUAL SURGICAL INSTRUMENT7 reports
- EXPEDIUM VERSE 199723435bone cement, posterior screw augmentation6 reports
- EXPEDIUM VERSE 199721430APPLIANCE, FIXATION, SPINAL INTERLAMINAL6 reports
- EXPEDIUM VERSE 199723540SAppliance, fixation, spinal intervertebral body6 reports
- EXPEDIUM VERSE 299704255ORTHOPEDIC MANUAL SURGICAL INSTRUMENT6 reports
- EXPEDIUM VERSE 2997-04-306ORTHOPEDIC MANUAL SURGICAL INSTRUMENT6 reports
- EXPEDIUM VERSE 199723635ORTHOSIS, SPINAL PEDICLE FIXATION5 reports
- EXPEDIUM VERSE 199723740bone cement, posterior screw augmentation4 reports
- EXPEDIUM VERSE 199723655bone cement, posterior screw augmentation4 reports
- EXPEDIUM VERSE 199723535bone cement, posterior screw augmentation4 reports
- EXPEDIUM VERSE 199721850Orthosis, spinal pedicle fixation, for degenerative disc disease4 reports
- EXPEDIUM VERSE 199721740ORTHOSIS, SPINAL PEDICLE FIXATION4 reports
- EXPEDIUM VERSE 199721525ORTHOSIS, SPINAL PEDICLE FIXATION4 reports
- EXPEDIUM VERSE 299704272ORTHOPEDIC MANUAL SURGICAL INSTRUMENT4 reports
- EXPEDIUM VERSE 199723850ORTHOSIS, SPINAL PEDICLE FIXATION3 reports
- EXPEDIUM VERSE 199723860SThoracolumbosacral pedicle screw system3 reports
- EXPEDIUM VERSE 199723735SAppliance, fixation, spinal intervertebral body3 reports
- EXPEDIUM VERSE 299704205ORTHOPEDIC MANUAL SURGICAL INSTRUMENT3 reports
- EXPEDIUM VERSE 199723840bone cement, posterior screw augmentation2 reports
- EXPEDIUM VERSE 199723540bone cement, posterior screw augmentation2 reports
- EXPEDIUM VERSE 199721435Orthosis, spinal pedicle fixation, for degenerative disc disease2 reports
- EXPEDIUM VERSE 199723530SAppliance, fixation, spinal intervertebral body2 reports
- EXPEDIUM VERSE 199723535SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL2 reports
- EXPEDIUM VERSE 199723630SThoracolumbosacral pedicle screw system2 reports
- EXPEDIUM VERSE 199723635SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL2 reports
- EXPEDIUM VERSE 199723880SThoracolumbosacral pedicle screw system2 reports
- EXPEDIUM VERSE 199723755SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL2 reports
- EXPEDIUM VERSE 199723435SThoracolumbosacral pedicle screw system2 reports
- EXPEDIUM VERSE 299704270ORTHOPEDIC MANUAL SURGICAL INSTRUMENT2 reports
- EXPEDIUM VERSE 299704815TRAY, SURGICAL, INSTRUMENT2 reports
- EXPEDIUM VERSE 199723760ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- EXPEDIUM VERSE 199723755bone cement, posterior screw augmentation1 report
- EXPEDIUM VERSE 199723630bone cement, posterior screw augmentation1 report
- EXPEDIUM VERSE 199723550bone cement, posterior screw augmentation1 report
- EXPEDIUM VERSE 199723530ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- EXPEDIUM VERSE 199723440bone cement, posterior screw augmentation1 report
- EXPEDIUM VERSE 199723430ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- EXPEDIUM VERSE 199721899Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- EXPEDIUM VERSE 199721890APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- EXPEDIUM VERSE 199721870Orthosis, spondylolisthesis spinal fixation1 report
- EXPEDIUM VERSE 199721760Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- EXPEDIUM VERSE 199721755Pedicle screw spinal system, adolescent idiopathic scoliosis1 report
- EXPEDIUM VERSE 199721735Pedicle screw spinal system, adolescent idiopathic scoliosis1 report
- EXPEDIUM VERSE 199721660Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- EXPEDIUM VERSE 199721425APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- EXPEDIUM VERSE 199723550SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- EXPEDIUM VERSE 199723845SThoracolumbosacral pedicle screw system1 report
- EXPEDIUM VERSE 199723840SAppliance, fixation, spinal intervertebral body1 report
- EXPEDIUM VERSE 199723730SThoracolumbosacral pedicle screw system1 report
- EXPEDIUM VERSE 299704165ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- EXPEDIUM VERSE 299704155PINSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT1 report
- EXPEDIUM VERSE 299704845TRAY, SURGICAL, INSTRUMENT1 report
- EXPEDIUM VERSE 299704152PINSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT1 report
- EXPEDIUM VERSE 299704230PINSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT1 report
Recent EXPEDIUM VERSE adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 25, 2026Break; Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50898824 ↗MalfunctionSep 22, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50859485 ↗MalfunctionSep 22, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50859484 ↗MalfunctionSep 22, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50859481 ↗MalfunctionSep 11, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50741439 ↗MalfunctionSep 11, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50741407 ↗MalfunctionSep 11, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50741205 ↗MalfunctionSep 11, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50741201 ↗MalfunctionAug 27, 2026Break
It was reported that X25 FINAL TIGHTENER, VERSE X25 INSERTER/TIGHTENER, and FINAL TIGHTENER X20 chipped too quickly and broke during use, including reports that tips broke inside the patient. The event was identified pre-operatively/intraoperatively during use. No patient harm or significant delay was reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50479512 ↗MalfunctionAug 27, 2026Break
It was reported that X25 FINAL TIGHTENER, VERSE X25 INSERTER/TIGHTENER, and FINAL TIGHTENER X20 chipped too quickly and broke during use, including reports that tips broke inside the patient. The event was identified pre-operatively/intraoperatively during use. No patient harm or significant delay was reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50479510 ↗MalfunctionAug 13, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50236992 ↗MalfunctionAug 13, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50236989 ↗MalfunctionAug 13, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50236985 ↗MalfunctionAug 12, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50228897 ↗MalfunctionAug 12, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50227551 ↗
Other Medos International Sàrl products
- TRUESPAN ORTHOCORD6 models · 4,109 reports
- FMS39 models · 3,588 reports
- EXPEDIUM291 models · 3,312 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
- GRYPHON ORTHOCORD6 models · 918 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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