OKTAGON Dental Implant BLT RC 24003Recalls & reported problems
Hager & Meisinger Gesellschaft mit beschränkter Haftung · Bone Level Tapered Implant Regular Connect Ø4.1 x 12mm · Class 2 · Implant
All models of OKTAGON Dental Implant BLT RC (6)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 11
- Deaths reported
- 0
- Injuries reported
- 11
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI E0HM240031), received between Jun 6, 2019 and Jun 2, 2022 — classified as 11 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (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.
Most reported problems
Device problems
- Failure to Osseointegrate10
- Fracture1
Patient problems
- Inadequate Osseointegration9
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 11 most recent of 11 reports, in the reporter's own words as published by the FDA.
InjuryJun 2, 2022Failure to Osseointegrate; Failure to Osseointegrate
MISSING OSSEOINTEGRATION, IMPLANT FALL OUT AFTER 3 WEEKS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14572697 ↗InjuryMar 9, 2022Fracture; Fracture
BREAKAGE OF TRANSFER SCREW DUE TO HIGH TORQUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13712369 ↗InjuryMar 1, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjurySep 30, 2021Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 2, 2021Failure to Osseointegrate; Failure to Osseointegrate
PRIMARY STABILITY WAS NOT ACHIEVED.
Patient problems: Inadequate Osseointegration
MAUDE report 12106077 ↗InjuryJul 24, 2020Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 18, 2019Failure to Osseointegrate; Failure to Osseointegrate
NO OSSEOINTEGRATION AFTER 4 MONTH, TYPE IV BONE.
Patient problems: Inadequate Osseointegration
MAUDE report 8801377 ↗InjuryJun 28, 2019Failure to Osseointegrate; Failure to Osseointegrate
OPENED, THEN DECIDED ON A 4.8MM IMPLANT.
Patient problems: Inadequate Osseointegration
MAUDE report 8743244 ↗InjuryJun 12, 2019Failure to Osseointegrate; Failure to Osseointegrate
PATIENT STATED THAT IMPLANT FELL OUT. WAS ALREADY OUT WHEN PAT. WAS IN CLINIC ON (B)(6) 2019.
Patient problems: Inadequate Osseointegration
MAUDE report 8690279 ↗InjuryJun 6, 2019Failure to Osseointegrate; Failure to Osseointegrate
NO OSSEOINTEGRATION WAS ACHIEVED.
Patient problems: Inadequate Osseointegration
MAUDE report 8674667 ↗InjuryJun 6, 2019Failure 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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