infinity OCTAGON Bone Level Taper Dental Implant BLT504810Recalls & reported problems
Hager & Meisinger Gesellschaft mit beschränkter Haftung · infinity OCTAGON Bone Level Taper Dental Implant 4.8x10 mm Regular Platform · Class 2 · Implant
All models of infinity OCTAGON Bone Level Taper Dental Implant (10)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 20
- Deaths reported
- 0
- Injuries reported
- 20
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 20 adverse event reports that list this exact device (DI E0HMBLT5048101), received between Aug 9, 2022 and Jun 14, 2024 — classified as 20 injuries.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (10 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, 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.
Reports received per month
Most reported problems
Device problems
- Patient Device Interaction Problem10
- Failure to Osseointegrate9
- Activation, Positioning or Separation Problem1
Patient problems
- Inadequate Osseointegration11
- Failure of Implant8
- Pain1
Recent adverse event reports
The 20 most recent of 20 reports, in the reporter's own words as published by the FDA.
InjuryJun 14, 2024Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryApr 11, 2024Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryMar 18, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 15, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 5, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjurySep 29, 2023Patient Device Interaction Problem; Patient Device Interaction Problem
InjurySep 26, 2023Patient Device Interaction Problem; Patient Device Interaction Problem
PAIN WITHIN ONE YEAR AFTER THE RESTORATION.
Patient problems: Failure of Implant
MAUDE report 17821899 ↗InjurySep 7, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjuryAug 30, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjuryAug 16, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjuryAug 16, 2023Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryAug 16, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjuryJun 2, 2023Activation, Positioning or Separation Problem; Activation, Positioning or Separation Problem
InjuryMay 24, 2023Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryApr 25, 2023Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryApr 20, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjuryApr 19, 2023Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryApr 19, 2023Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryMar 28, 2023Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryAug 9, 2022Failure to Osseointegrate; Failure to Osseointegrate
Other Implant, Endosseous, Root-Form devices
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM43,616 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM40,404 reports
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM27,400 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM25,621 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM25,298 reports
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM23,448 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,320 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,267 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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