SYMPHONYRecalls & reported problems across all models
Medos International Sàrl · 113 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 860
- Deaths reported
- 14
- Injuries reported
- 70
- Recalls
- 0
We found 113 models of SYMPHONY by Medos International Sàrl in the FDA's device registry (GUDID). Together they are named in 860 adverse event reports in the FDA's MAUDE database, received between Dec 3, 2019 and Sep 29, 2026 — classified as 14 deaths, 70 injuries, 776 malfunctions.
The most frequently reported specific device problem is “Material Twisted/Bent” (308 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 SYMPHONY problems
Device problems
- Material Twisted/Bent308
- Device-Device Incompatibility243
- Break176
- Material Deformation72
- Calibration Problem59
- Adverse Event Without Identified Device or Use Problem26
- Failure to Cut23
- Migration22
Patient problems
- No Clinical Signs, Symptoms or Conditions701
- Insufficient Information44
- No Consequences Or Impact To Patient36
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available19
- Foreign Body In Patient17
- Unspecified Tissue Injury16
- Nonunion/Delayed-union Bone Fracture11
- Pain9
SYMPHONY models
113 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- SYMPHONY 2020-00-403DRIVER, PROSTHESIS173 reports
- SYMPHONY 2020-00-407DRIVER, PROSTHESIS103 reports
- SYMPHONY 2020-33-400Orthopedic stereotaxic instrument95 reports
- SYMPHONY 2020-00-504ORTHOPEDIC MANUAL SURGICAL INSTRUMENT58 reports
- SYMPHONY 2020-00-401Orthopedic stereotaxic instrument53 reports
- SYMPHONY 2020-00-120Orthopedic stereotaxic instrument36 reports
- SYMPHONY 2020-00-135INSTRUMENT, CUTTING, ORTHOPEDIC20 reports
- SYMPHONY 2020-00-140ORTHOPEDIC MANUAL SURGICAL INSTRUMENT19 reports
- SYMPHONY 1020-35-112Posterior cervical screw system6 deaths15 reports
- SYMPHONY 1020-35-116SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL14 reports
- SYMPHONY 1020-00-000APPLIANCE, FIXATION, SPINAL INTERLAMINAL11 reports
- SYMPHONY 1020-00-000SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL11 reports
- SYMPHONY 2020-00-123Orthopedic stereotaxic instrument11 reports
- SYMPHONY 2020-00-141ORTHOPEDIC MANUAL SURGICAL INSTRUMENT10 reports
- SYMPHONY 1020-19-004Posterior cervical screw system9 reports
- SYMPHONY 2020-00-330BIT, DRILL8 reports
- SYMPHONY 2020-00-335BIT, DRILL8 reports
- SYMPHONY 3010-19-011Orthopedic stereotaxic instrument8 reports
- SYMPHONY 1020-35-116Posterior cervical screw system6 reports
- SYMPHONY 1020-24-004SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL6 reports
- SYMPHONY 2020-00-154INSTRUMENT, CUTTING, ORTHOPEDIC6 reports
- SYMPHONY 2020-00-501ORTHOPEDIC MANUAL SURGICAL INSTRUMENT6 reports
- SYMPHONY 2020-00-500ORTHOPEDIC MANUAL SURGICAL INSTRUMENT6 reports
- SYMPHONY 1020-40-118APPLIANCE, FIXATION, SPINAL INTERLAMINAL2 deaths5 reports
- SYMPHONY 1020-23-102SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL5 reports
- SYMPHONY 2020-00-119ORTHOPEDIC MANUAL SURGICAL INSTRUMENT5 reports
- SYMPHONY 1020-15-111Posterior cervical screw system4 reports
- SYMPHONY 1020-35-110SPosterior cervical screw system4 reports
- SYMPHONY 2020-00-145BENDER4 reports
- SYMPHONY 2020-33-401Orthopedic stereotaxic instrument4 reports
- SYMPHONY 2020-33-330Orthopedic stereotaxic instrument4 reports
- SYMPHONY 2020-33-335Orthopedic stereotaxic instrument4 reports
- SYMPHONY 2020-00-410CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY4 reports
- SYMPHONY 1020-40-116Posterior cervical screw system3 reports
- SYMPHONY 1020-24-003SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL3 reports
- SYMPHONY 1020-74-220SPosterior cervical screw system3 reports
- SYMPHONY 1020-35-114SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL3 reports
- SYMPHONY 1020-35-130SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL3 reports
- SYMPHONY 1020-35-316SPosterior cervical screw system3 reports
- SYMPHONY 2020-00-117CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY3 reports
- SYMPHONY 2020-00-118Orthopedic stereotaxic instrument3 reports
- SYMPHONY 2020-00-224Orthopedic stereotaxic instrument3 reports
- SYMPHONY 2020-00-239Guide, surgical, instrument3 reports
- SYMPHONY 2020-00-244Guide, surgical, instrument3 reports
- SYMPHONY 1020-45-224Posterior cervical screw system2 deaths2 reports
- SYMPHONY 1020-64-075Posterior cervical screw system2 deaths2 reports
- SYMPHONY 1020-40-114Posterior cervical screw system2 reports
- SYMPHONY 1020-35-728Posterior cervical screw system2 reports
- SYMPHONY 1020-13-240APPLIANCE, FIXATION, SPINAL INTERLAMINAL2 reports
- SYMPHONY 1020-24-004Posterior cervical screw system2 reports
- SYMPHONY 1020-23-101SPosterior cervical screw system2 reports
- SYMPHONY 1020-24-002SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL2 reports
- SYMPHONY 1020-24-005SPosterior cervical screw system2 reports
- SYMPHONY 1020-15-083SPosterior cervical screw system2 reports
- SYMPHONY 1020-45-222SPosterior cervical screw system2 reports
- SYMPHONY 1020-45-110SPosterior cervical screw system2 reports
- SYMPHONY 1020-35-112SPosterior cervical screw system2 reports
- SYMPHONY 1020-35-128SPosterior cervical screw system2 reports
- SYMPHONY 1020-35-132SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL2 reports
- SYMPHONY 1020-35-312SPosterior cervical screw system2 reports
- SYMPHONY 1020-40-116SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL2 reports
- SYMPHONY 1020-40-118SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL2 reports
- SYMPHONY 1020-40-126SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL2 reports
- SYMPHONY 2020-00-138DRIVER, PROSTHESIS2 reports
- SYMPHONY 2020-33-140Orthopedic stereotaxic instrument2 reports
- SYMPHONY 2020-00-405DRIVER, PROSTHESIS2 reports
- SYMPHONY 3010-19-012Orthopedic stereotaxic instrument2 reports
- SYMPHONY 1020-35-114APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-35-120APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-35-128Posterior cervical screw system1 report
- SYMPHONY 1020-35-130APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-45-226Posterior cervical screw system1 report
- SYMPHONY 1020-63-080Posterior cervical screw system1 death1 report
- SYMPHONY 1020-63-085APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 death1 report
- SYMPHONY 1020-40-128APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-40-130APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-35-730Posterior cervical screw system1 report
- SYMPHONY 1020-35-734APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-23-002APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-21-351APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-21-401APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-14-240SPosterior cervical screw system1 report
- SYMPHONY 1020-21-403SPosterior cervical screw system1 report
- SYMPHONY 1020-23-103SPosterior cervical screw system1 report
- SYMPHONY 1020-21-402SPosterior cervical screw system1 report
- SYMPHONY 1020-21-401SPosterior cervical screw system1 report
- SYMPHONY 1020-30-114SPosterior cervical screw system1 report
- SYMPHONY 1020-40-328SPosterior cervical screw system1 report
- SYMPHONY 1020-35-728SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-45-226SPosterior cervical screw system1 report
- SYMPHONY 1020-50-228SPosterior cervical screw system1 report
- SYMPHONY 1020-84-600SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-64-050SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-64-055SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-35-118SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-35-120SPosterior cervical screw system1 report
- SYMPHONY 1020-50-428SPosterior cervical screw system1 report
- SYMPHONY 1020-55-234SPosterior cervical screw system1 report
- SYMPHONY 1020-35-314SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-40-112SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
Recent SYMPHONY adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50936704 ↗MalfunctionSep 29, 2026Material Twisted/Bent
It was reported that the X15 DRIVER FINAL TIGHTENER worn down
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50929632 ↗MalfunctionSep 29, 2026Material Twisted/Bent
It was reported that the X15 DRIVER FINAL TIGHTENER worn down.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50929630 ↗MalfunctionSep 29, 2026Material Twisted/Bent
It was reported that the X15 DRIVER FINAL TIGHTENER worn down.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50929629 ↗MalfunctionSep 29, 2026Material Twisted/Bent
It was reported that the X15 DRIVER FINAL TIGHTENER worn down.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50929628 ↗MalfunctionSep 23, 2026Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50868408 ↗MalfunctionSep 22, 2026Break; Entrapment of Device
Patient problems: Foreign Body In Patient
MAUDE report 50860156 ↗MalfunctionSep 22, 2026Break; Material Twisted/Bent
It was reported that the Symphony final tightener was stripped/broken. There was no patient harm or surgical delay.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50856166 ↗MalfunctionSep 17, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50810298 ↗MalfunctionSep 15, 2026Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50781555 ↗MalfunctionSep 15, 2026Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50781553 ↗MalfunctionSep 15, 2026Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50781552 ↗MalfunctionSep 15, 2026Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50781548 ↗MalfunctionSep 8, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50677505 ↗MalfunctionSep 8, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50675190 ↗
Other Medos International Sàrl products
- TRUESPAN ORTHOCORD6 models · 4,109 reports
- FMS39 models · 3,588 reports
- EXPEDIUM291 models · 3,312 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
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.
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