infinity OCTAGONRecalls & reported problems across all models
Hager & Meisinger Gesellschaft mit beschränkter Haftung · 21 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 509
- Deaths reported
- 0
- Injuries reported
- 504
- Recalls
- 0
We found 21 models of infinity OCTAGON by Hager & Meisinger Gesellschaft mit beschränkter Haftung in the FDA's device registry (GUDID). Together they are named in 509 adverse event reports in the FDA's MAUDE database, received between Mar 13, 2019 and Apr 1, 2026 — classified as 504 injuries, 5 malfunctions.
The most frequently reported specific device problem is “Failure to Osseointegrate” (284 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 infinity OCTAGON problems
Device problems
- Failure to Osseointegrate284
- Patient Device Interaction Problem96
- Osseointegration Problem92
- Loss of Osseointegration90
- Fracture8
- Insufficient Device Problem Information5
- Loosening of Implant Not Related to Bone-Ingrowth5
- Adverse Event Without Identified Device or Use Problem2
Patient problems
- Failure of Implant300
- Inadequate Osseointegration203
- Pain13
- Unspecified Infection8
- No Clinical Signs, Symptoms or Conditions4
- Swelling4
- Fistula2
- Insufficient Information2
infinity OCTAGON models
21 models, most reported first. Each model has its own page with its reports, recalls and device details.
- infinity OCTAGON 504110Implant, Endosseous, Root-Form98 reports
- infinity OCTAGON 503310Implant, Endosseous, Root-Form92 reports
- infinity OCTAGON 504810WPImplant, Endosseous, Root-Form47 reports
- infinity OCTAGON 504110BLImplant, Endosseous, Root-Form32 reports
- infinity OCTAGON 504108Implant, Endosseous, Root-Form29 reports
- infinity OCTAGON 503308Implant, Endosseous, Root-Form24 reports
- infinity OCTAGON 504810Implant, Endosseous, Root-Form24 reports
- infinity OCTAGON 504810BLImplant, Endosseous, Root-Form24 reports
- infinity OCTAGON 504108BLImplant, Endosseous, Root-Form23 reports
- infinity OCTAGON 503310BLImplant, Endosseous, Root-Form21 reports
- infinity OCTAGON 504808WPImplant, Endosseous, Root-Form20 reports
- infinity OCTAGON 504112BLImplant, Endosseous, Root-Form17 reports
- infinity OCTAGON 504812BLImplant, Endosseous, Root-Form12 reports
- infinity OCTAGON 503308BLImplant, Endosseous, Root-Form11 reports
- infinity OCTAGON 504808BLImplant, Endosseous, Root-Form11 reports
- infinity OCTAGON 503312BLImplant, Endosseous, Root-Form7 reports
- infinity OCTAGON 504112Implant, Endosseous, Root-Form7 reports
- infinity OCTAGON 504808Implant, Endosseous, Root-Form5 reports
- infinity OCTAGON 503312Implant, Endosseous, Root-Form2 reports
- infinity OCTAGON 504812WPImplant, Endosseous, Root-Form2 reports
- infinity OCTAGON 504114BLImplant, Endosseous, Root-Form1 report
Recent infinity OCTAGON adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryApr 1, 2026Failure to Osseointegrate
InjuryAug 12, 2025Osseointegration Problem; Osseointegration Problem
InjuryJun 27, 2025Osseointegration Problem; Osseointegration Problem
InjuryApr 30, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryMar 24, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryMar 24, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryMar 24, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryMar 24, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryMar 24, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryMar 24, 2025Fracture; Fracture
InjuryMar 24, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 24, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryMar 19, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 19, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 19, 2025Failure to Osseointegrate; Failure to Osseointegrate
Other Hager & Meisinger Gesellschaft mit beschränkter Haftung products
All Hager & Meisinger Gesellschaft mit beschränkter Haftung devices →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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