OKTAGON Dental Implant BL RC 22007Recalls & reported problems
Hager & Meisinger Gesellschaft mit beschränkter Haftung · Bone Level Implant Regular Connect Ø4.8x12mm · Class 2 · Implant
All models of OKTAGON Dental Implant BL RC (7)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 9
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI E0HM220071), received between Apr 18, 2019 and Jul 15, 2022 — classified as 9 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (8 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.
Most reported problems
Device problems
- Failure to Osseointegrate8
- Patient Device Interaction Problem1
Patient problems
- Inadequate Osseointegration7
- Failure of Implant1
- Pain1
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
InjuryJul 15, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 1, 2022Patient Device Interaction Problem; Patient Device Interaction Problem
FAILURE DURING IMPLANTATION, HIGH TORQUE WAS RECOGNIZED, THE IMPLANT SURFACE WASN'T COMPLETELY COVERED WITH BONE.
Patient problems: Failure of Implant
MAUDE report 13635164 ↗InjuryApr 28, 2021Failure to Osseointegrate; Failure to Osseointegrate
SURGEON NEEDED A LONGER IMPLANT.
Patient problems: Inadequate Osseointegration
MAUDE report 11736636 ↗InjuryApr 28, 2021Failure to Osseointegrate; Failure to Osseointegrate
SURGEON NEEDED A DIFFERENT SIZE.
Patient problems: Inadequate Osseointegration
MAUDE report 11736630 ↗InjuryJul 24, 2020Failure to Osseointegrate; Failure to Osseointegrate
IMPLANT DIDN'T ACHIEVED PRIMARY STABILITY IN SURGERY.
Patient problems: Inadequate Osseointegration
MAUDE report 10318492 ↗InjuryJun 17, 2019Failure to Osseointegrate; Failure to Osseointegrate
IMPLANT WAS SPINNING AT TIME OF PLACEMENT.
Patient problems: Inadequate Osseointegration
MAUDE report 8703149 ↗InjuryMay 20, 2019Failure to Osseointegrate; Failure to Osseointegrate
INADEQUATE BONE QUALITY FOR IMPLANT PLACEMENT.
Patient problems: Inadequate Osseointegration
MAUDE report 8623424 ↗InjuryMay 20, 2019Failure to Osseointegrate; Failure to Osseointegrate
IMPLANT HAS TO BE REMOVED AFTER 12 DAYS DUE TO SEVERE PAIN AFTER PLACEMENT.
Patient problems: Pain
MAUDE report 8623276 ↗InjuryApr 18, 2019Failure to Osseointegrate; Failure to Osseointegrate
IMPLANT DID NOT ACHIEVE PRIMARY STABILITY DUE TO AN INADEQUATE BONE-QUALITY/-QUANTITY.
Patient problems: Inadequate Osseointegration
MAUDE report 8526338 ↗
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- 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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