Touareg™-OS Dental Implant 4.2D 10L ISF1042Recalls & reported problems
Adin Dental Implant Systems Ltd · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 8
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 07290105151377), received between Apr 23, 2023 and Jun 2, 2026 — classified as 8 injuries.
The most frequently reported specific device problem is “Osseointegration Problem” (6 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
- Osseointegration Problem6
- Fracture2
- Patient Device Interaction Problem1
Patient problems
- Inadequate Osseointegration4
- Bacterial Infection3
- Pain3
- Failure of Implant2
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
InjuryJun 2, 2026Patient Device Interaction Problem
InjuryMay 21, 2026Osseointegration Problem
MOBILITY 4 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 25244213 ↗InjuryFeb 10, 2026Osseointegration Problem
PAIN, INFECTION AND MOBILITY 1 MONTHS AFTER IMPLANTATION PATIENT WITH PARKISON DISEASE.
Patient problems: Bacterial Infection; Inadequate Osseointegration; Pain
MAUDE report 24305534 ↗InjuryJun 12, 2025Osseointegration Problem; Osseointegration Problem
PAIN AND MOBILITY 5 MONTHS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Inadequate Osseointegration
MAUDE report 22197033 ↗InjuryJun 12, 2025Osseointegration Problem; Osseointegration Problem
InjuryJan 17, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY AND INFECTION 4 MONTH AFTER IMPLANTATION, IMPLANT REMOVED AND BONE GRAFT PLACED.
Patient problems: Bacterial Infection; Inadequate Osseointegration
MAUDE report 21179801 ↗InjuryApr 24, 2023Fracture; Osseointegration Problem; Fracture; Osseointegration Problem
THE CLINICIAN REPORTS IMPLANT FRACTURE. NO FURTHER PATIENT COMPLICATIONS WERE REPORTED.
Patient problems: Failure of Implant
MAUDE report 16797098 ↗InjuryApr 23, 2023Fracture; Fracture
THE CLINICIAN REPORTS IMPLANT FRACTURE. NO FURTHER PATIENT COMPLICATIONS WERE REPORTED.
Patient problems: Failure of Implant
MAUDE report 16792778 ↗
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- 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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