infinity OCTAGON Bone Level Taper Dental Implant BLT504110Recalls & reported problems
Hager & Meisinger Gesellschaft mit beschränkter Haftung · infinity OCTAGON Bone Level Taper Dental Implant 4.1x10 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
Quick summary
This Hager & Meisinger infinity OCTAGON bone-level dental implant is a screw-shaped implant used to replace missing teeth in the jaw. The 28 reports mostly describe implants that fail to fuse with the bone, lose that bond later, or come loose and have to be removed, with one report of the carrier breaking inside the implant during placement. All 28 reports describe injuries, and no deaths were reported. There are no recalls naming this device, and no reports were filed in the past 12 months.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 28
- Deaths reported
- 0
- Injuries reported
- 28
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 28 adverse event reports that list this exact device (DI E0HMBLT5041101), received between Feb 9, 2021 and Apr 12, 2024 — classified as 28 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (17 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 Osseointegrate17
- Patient Device Interaction Problem8
- Osseointegration Problem5
- Activation, Positioning or Separation Problem1
- Inadequacy of Device Shape and/or Size1
- Loss of Osseointegration1
Patient problems
- Inadequate Osseointegration15
- Failure of Implant13
Recent adverse event reports
The 25 most recent of 28 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 19099691 ↗InjuryApr 12, 2024Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryApr 12, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryFeb 13, 2024Loss of Osseointegration; Loss of Osseointegration
InjuryDec 11, 2023Failure to Osseointegrate; Failure to Osseointegrate
PATIENT WAS IN FOR A POST-OP VISIT AND IMPLANT WAS REMOVED DUE TO MOBILITY.
Patient problems: Failure of Implant
MAUDE report 18307550 ↗InjuryNov 9, 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 18102994 ↗InjuryOct 5, 2023Patient Device Interaction Problem; Patient Device Interaction Problem
InjurySep 29, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjurySep 29, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjurySep 27, 2023Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryAug 10, 2023Patient Device Interaction Problem; Patient Device Interaction Problem
MISSING OSSEOINTEGRATION AS REMOVAL OF TRANSFER PART WAS NOT POSSIBLE.
Patient problems: Inadequate Osseointegration
MAUDE report 17498376 ↗InjuryJul 7, 2023Inadequacy of Device Shape and/or Size; Inadequacy of Device Shape and/or Size
HAD TO CHANGE IMPLANT SIZE TO ACHIEVE STABILITY.
Patient problems: Failure of Implant
MAUDE report 17277115 ↗InjuryMay 23, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjuryApr 20, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjuryApr 19, 2023Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryApr 19, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjuryApr 19, 2023Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryMar 20, 2023Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryMar 20, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjuryDec 2, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryDec 2, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryNov 22, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryNov 22, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryFeb 10, 2021Failure to Osseointegrate; Osseointegration Problem; Failure to Osseointegrate; Osseointegration Problem
DOCTOR NEEDED BIGGER IMPLANT WAS 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 PERFORMED AT THE TIME OF SURGERY.
Patient problems: Failure of Implant
MAUDE report 11310862 ↗InjuryFeb 10, 2021Failure to Osseointegrate; Osseointegration Problem; Failure to Osseointegrate; Osseointegration Problem
ASYMPTOMATIC WAS REPORTED. BONE QUALITY AT THE TIME OF IMPLANT FAILURE TYPE III. TIME OF LOSS IN RELATION TO THE IMPLANTATION WAS BEFORE PROSTHETIC RESTORATION. PRIMARY STABILITY AND OSSEOINTEGRATION WAS NOT ACHIEVE. AUGMENTATION PROCEDURE WAS NOT PERFORMED AT THE TIME OF SURGERY.
Patient problems: Failure of Implant
MAUDE report 11310666 ↗
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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