infinity OCTAGON Bone Level Taper Dental Implant BLT503310Recalls & reported problems
Hager & Meisinger Gesellschaft mit beschränkter Haftung · infinity OCTAGON Bone Level Taper Dental Implant 3.3x10 mm Narrow 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
- 10
- Deaths reported
- 0
- Injuries reported
- 10
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI E0HMBLT5033101), received between Feb 8, 2021 and Apr 12, 2024 — classified as 10 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (7 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
- Failure to Osseointegrate7
- Patient Device Interaction Problem3
- Osseointegration Problem2
- Activation, Positioning or Separation Problem1
Patient problems
- Inadequate Osseointegration6
- Failure of Implant4
Recent adverse event reports
The 10 most recent of 10 reports, in the reporter's own words as published by the FDA.
InjuryApr 12, 2024Patient Device Interaction Problem; Patient Device Interaction Problem
MISSING OSSEOINTEGRATION AS TRANSFER PART BROKE DURING INSERTION.
Patient problems: Inadequate Osseointegration
MAUDE report 19099764 ↗InjuryNov 8, 2023Activation, Positioning or Separation Problem; Activation, Positioning or Separation Problem
IMPLANT CARRIER BROKE INSIDE IMPLANT DURING SURGICAL PLACEMENT.
Patient problems: Failure of Implant
MAUDE report 18097059 ↗InjuryAug 14, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 14, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjuryMay 24, 2023Failure to Osseointegrate; Osseointegration Problem; Patient Device Interaction Problem; Failure to Osseointegrate; Osseointegration Problem; Patient Device Interaction Problem
InjuryApr 25, 2023Patient Device Interaction Problem; Patient Device Interaction Problem
BUCCAL BONE LOSS AT UNCOVERY STAGE. PREVIOUS FAILING IMPLANT.
Patient problems: Failure of Implant
MAUDE report 16808684 ↗InjuryMar 7, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 1, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryMay 19, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryFeb 8, 2021Failure to Osseointegrate; Osseointegration Problem; Failure to Osseointegrate; Osseointegration Problem
DOCTOR NEEDED A WIDER IMPLANT AND MOBILITY WERE REPORTED. BONE QUALITY AT THE TIME OF IMPLANT FAILURE TYPE II. TIME OF LOSS IN RELATION TO THE IMPLANTATION WAS BEFORE PROSTHETIC RESTORATION. PRIMARY STABILITY AND OSSEOINTEGRATION WAS NOT ACHIEVED. AUGMENTATION PROCEDURE WAS NOT PERFORMED AT THE TIME OF SURGERY.
Patient problems: Failure of Implant
MAUDE report 11296665 ↗
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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