EXPEDIUMRecalls & reported problems across all models
Medos International Sàrl · 291 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3,312
- Deaths reported
- 0
- Injuries reported
- 1,107
- Recalls
- 0
We found 291 models of EXPEDIUM by Medos International Sàrl in the FDA's device registry (GUDID). Together they are named in 3,312 adverse event reports in the FDA's MAUDE database, received between Apr 30, 2014 and Sep 30, 2026 — classified as 1,107 injuries, 2,205 malfunctions.
The most frequently reported specific device problem is “Break” (1,180 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 problems
Device problems
- Break1,180
- Material Twisted/Bent597
- Adverse Event Without Identified Device or Use Problem340
- Device-Device Incompatibility319
- Loose or Intermittent Connection176
- Contamination /Decontamination Problem151
- Device Slipped133
- Material Deformation117
Patient problems
- No Clinical Signs, Symptoms or Conditions1,653
- No Consequences Or Impact To Patient410
- No Code Available218
- Insufficient Information157
- Failure of Implant130
- Foreign Body In Patient126
- Pain121
- Not Applicable102
EXPEDIUM models
291 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- EXPEDIUM 279712400SCREWDRIVER551 reports
- EXPEDIUM 179702000APPLIANCE, FIXATION, SPINAL INTERLAMINAL439 reports
- EXPEDIUM 299704320ORTHOPEDIC MANUAL SURGICAL INSTRUMENT144 reports
- EXPEDIUM 3010-19-003Orthopedic stereotaxic instrument133 reports
- EXPEDIUM 279726401ORTHOPEDIC MANUAL SURGICAL INSTRUMENT125 reports
- EXPEDIUM 179762480Pedicle screw spinal system, adolescent idiopathic scoliosis114 reports
- EXPEDIUM 279702050SCREWDRIVER107 reports
- EXPEDIUM 279734000NOrthopedic stereotaxic instrument84 reports
- EXPEDIUM 279712580CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY69 reports
- EXPEDIUM 179702000SOrthosis, spinal pedicle fixation, for degenerative disc disease52 reports
- EXPEDIUM 310002155PINSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT52 reports
- EXPEDIUM 279712570ORTHOPEDIC MANUAL SURGICAL INSTRUMENT45 reports
- EXPEDIUM 279726500DISPENSER, CEMENT44 reports
- EXPEDIUM 279730145ORTHOPEDIC MANUAL SURGICAL INSTRUMENT44 reports
- EXPEDIUM 279722400SCREWDRIVER40 reports
- EXPEDIUM 299704310ORTHOPEDIC MANUAL SURGICAL INSTRUMENT39 reports
- EXPEDIUM 279712590DRIVER, PROSTHESIS38 reports
- EXPEDIUM 179902000ORTHOSIS, SPINAL PEDICLE FIXATION37 reports
- EXPEDIUM 179712645ORTHOSIS, SPINAL PEDICLE FIXATION33 reports
- EXPEDIUM 179712650Orthosis, spondylolisthesis spinal fixation31 reports
- EXPEDIUM 179712750ORTHOSIS, SPINAL PEDICLE FIXATION30 reports
- EXPEDIUM 286210130DRIVER, PROSTHESIS29 reports
- EXPEDIUM 179712640Pedicle screw spinal system, adolescent idiopathic scoliosis28 reports
- EXPEDIUM 279712550DRIVER, PROSTHESIS27 reports
- EXPEDIUM 179722000APPLIANCE, FIXATION, SPINAL INTERLAMINAL23 reports
- EXPEDIUM 179712745Orthosis, spondylolisthesis spinal fixation19 reports
- EXPEDIUM 179762300ORTHOSIS, SPINAL PEDICLE FIXATION19 reports
- EXPEDIUM 179788635Pedicle screw spinal system, adolescent idiopathic scoliosis18 reports
- EXPEDIUM 279702000DRIVER, PROSTHESIS18 reports
- EXPEDIUM 279703140ORTHOPEDIC MANUAL SURGICAL INSTRUMENT17 reports
- EXPEDIUM 179712740APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY16 reports
- EXPEDIUM 287720170DRIVER, PROSTHESIS16 reports
- EXPEDIUM 179788640APPLIANCE, FIXATION, SPINAL INTERLAMINAL14 reports
- EXPEDIUM 3010-19-006Orthopedic stereotaxic instrument14 reports
- EXPEDIUM 279712830SCREWDRIVER13 reports
- EXPEDIUM 279702600NOrthopedic stereotaxic instrument11 reports
- EXPEDIUM 299704315ORTHOPEDIC MANUAL SURGICAL INSTRUMENT11 reports
- EXPEDIUM 179712735ORTHOSIS, SPINAL PEDICLE FIXATION10 reports
- EXPEDIUM 179788530APPLIANCE, FIXATION, SPINAL INTERLAMINAL10 reports
- EXPEDIUM 279703120ORTHOPEDIC MANUAL SURGICAL INSTRUMENT10 reports
- EXPEDIUM 279702400NOrthopedic stereotaxic instrument10 reports
- EXPEDIUM 279702700NOrthopedic stereotaxic instrument10 reports
- EXPEDIUM 279702800NOrthopedic stereotaxic instrument10 reports
- EXPEDIUM 279702070PROBE9 reports
- EXPEDIUM 279702150ORTHOPEDIC MANUAL SURGICAL INSTRUMENT9 reports
- EXPEDIUM 286200240ORTHOPEDIC MANUAL SURGICAL INSTRUMENT9 reports
- EXPEDIUM 279702030NOrthopedic stereotaxic instrument9 reports
- EXPEDIUM 299704190BENDER9 reports
- EXPEDIUM 299704175ORTHOPEDIC MANUAL SURGICAL INSTRUMENT9 reports
- EXPEDIUM 299704195BENDER9 reports
- EXPEDIUM 299704200BENDER9 reports
- EXPEDIUM 3010-19-004Orthopedic stereotaxic instrument9 reports
- EXPEDIUM 179712045Orthosis, spinal pedicle fixation, for degenerative disc disease8 reports
- EXPEDIUM 179712635Orthosis, spinal pedicle fixation, for degenerative disc disease8 reports
- EXPEDIUM 179712880APPLIANCE, FIXATION, SPINAL INTERLAMINAL8 reports
- EXPEDIUM 179762120Orthosis, spinal pedicle fixation, for degenerative disc disease8 reports
- EXPEDIUM 279702140ORTHOPEDIC MANUAL SURGICAL INSTRUMENT8 reports
- EXPEDIUM 279726509CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY8 reports
- EXPEDIUM 299704125PROBE8 reports
- EXPEDIUM 299704185BENDER8 reports
- EXPEDIUM 299704135ORTHOPEDIC MANUAL SURGICAL INSTRUMENT8 reports
- EXPEDIUM 279729930INSTRUMENT, CUTTING, ORTHOPEDIC7 reports
- EXPEDIUM 299704145ORTHOPEDIC MANUAL SURGICAL INSTRUMENT7 reports
- EXPEDIUM 179702645Orthosis, spinal pedicle fixation, for degenerative disc disease6 reports
- EXPEDIUM 179712655Orthosis, spondylolisthesis spinal fixation6 reports
- EXPEDIUM 179712980Orthosis, spondylolisthesis spinal fixation6 reports
- EXPEDIUM 179715645Pedicle screw spinal system, adolescent idiopathic scoliosis6 reports
- EXPEDIUM 179722640APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY6 reports
- EXPEDIUM 179732740APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY6 reports
- EXPEDIUM 179755155APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY6 reports
- EXPEDIUM 179762060APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY6 reports
- EXPEDIUM 179788535Orthosis, spondylolisthesis spinal fixation6 reports
- EXPEDIUM 179788645ORTHOSIS, SPINAL PEDICLE FIXATION6 reports
- EXPEDIUM 179963600ORTHOSIS, SPINAL PEDICLE FIXATION6 reports
- EXPEDIUM 179988645ORTHOSIS, SPINAL PEDICLE FIXATION6 reports
- EXPEDIUM 279702080EXTRACTOR6 reports
- EXPEDIUM 279712150SCREWDRIVER6 reports
- EXPEDIUM 279702500NOrthopedic stereotaxic instrument6 reports
- EXPEDIUM 299704060TAP, BONE6 reports
- EXPEDIUM 299704130PROBE6 reports
- EXPEDIUM 2797-22-940ORTHOPEDIC MANUAL SURGICAL INSTRUMENT6 reports
- EXPEDIUM 179712850Orthosis, spondylolisthesis spinal fixation5 reports
- EXPEDIUM 179715640Orthosis, spinal pedicle fixation, for degenerative disc disease5 reports
- EXPEDIUM 179762045Orthosis, spondylolisthesis spinal fixation5 reports
- EXPEDIUM 179799645APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY5 reports
- EXPEDIUM 279702120ORTHOPEDIC MANUAL SURGICAL INSTRUMENT5 reports
- EXPEDIUM 279722460ORTHOPEDIC MANUAL SURGICAL INSTRUMENT5 reports
- EXPEDIUM 279722550DRIVER, PROSTHESIS5 reports
- EXPEDIUM 196791385Orthosis, spinal pedicle fixation, for degenerative disc disease5 reports
- EXPEDIUM 279718101DRIVER, PROSTHESIS5 reports
- EXPEDIUM 299704960TAP, BONE5 reports
- EXPEDIUM 279703140PINSTRUMENT, MANUAL, SURGICAL, GENERAL USE5 reports
- EXPEDIUM 279703150PINSTRUMENT, MANUAL, SURGICAL, GENERAL USE5 reports
- EXPEDIUM 179712530Pedicle screw spinal system, adolescent idiopathic scoliosis4 reports
- EXPEDIUM 179712545APPLIANCE, FIXATION, SPINAL INTERLAMINAL4 reports
- EXPEDIUM 179712755APPLIANCE, FIXATION, SPINAL INTERLAMINAL4 reports
- EXPEDIUM 179712990APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY4 reports
- EXPEDIUM 179722880APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY4 reports
- EXPEDIUM 179732640Orthosis, spondylolisthesis spinal fixation4 reports
- EXPEDIUM 179732645Pedicle screw spinal system, adolescent idiopathic scoliosis4 reports
Recent EXPEDIUM adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Break
It was reported the screwdriver tip broke off on an unknown date. No patient harm.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50944659 ↗MalfunctionSep 24, 2026Calibration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50889558 ↗MalfunctionSep 23, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50873873 ↗InjurySep 17, 2026Device Slipped
Patient problems: Insufficient Information
MAUDE report 50808477 ↗MalfunctionSep 11, 2026Device Slipped
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50742686 ↗MalfunctionSep 11, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50741412 ↗MalfunctionSep 11, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50741202 ↗MalfunctionSep 10, 2026Calibration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50718490 ↗MalfunctionSep 10, 2026Calibration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50718487 ↗MalfunctionSep 8, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50677034 ↗MalfunctionAug 28, 2026Scratched Material
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50503233 ↗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 50479596 ↗MalfunctionAug 19, 2026Break
It was reported the screwdriver tip broke off during screw insertion. No patient harm. No surgical delay.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50319699 ↗MalfunctionAug 13, 2026Contamination /Decontamination Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50233117 ↗MalfunctionAug 13, 2026Contamination /Decontamination Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50233114 ↗
Other Medos International Sàrl products
- TRUESPAN ORTHOCORD6 models · 4,109 reports
- FMS39 models · 3,588 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
- 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page