Touareg™-S Dental Implant 5.0D 11.5L ISPS1150Recalls & reported problems
Adin Dental Implant Systems Ltd · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 12
- Deaths reported
- 0
- Injuries reported
- 12
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 12 adverse event reports that list this exact device (DI 07290105151889), received between Sep 17, 2024 and Sep 6, 2026 — classified as 12 injuries.
The most frequently reported specific device problem is “Osseointegration Problem” (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.
Reports received per month
Most reported problems
Device problems
- Osseointegration Problem8
- Patient Device Interaction Problem3
- Loss of Osseointegration2
Patient problems
- Inadequate Osseointegration7
- Failure of Implant4
- Granuloma3
- Bacterial Infection2
- Unspecified Infection2
- Pain1
Recent adverse event reports
The 12 most recent of 12 reports, in the reporter's own words as published by the FDA.
InjurySep 6, 2026Osseointegration Problem; Patient Device Interaction Problem
Patient problems: Failure of Implant; Unspecified Infection
MAUDE report 50637913 ↗InjuryApr 28, 2026Loss of Osseointegration
MOBILITY 3 YEARS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 25020511 ↗InjuryFeb 3, 2026Osseointegration Problem
GRANULOMA 2 WEEKS AFTER IMPLANTATION.
Patient problems: Granuloma; Inadequate Osseointegration
MAUDE report 24246798 ↗InjuryFeb 2, 2026Patient Device Interaction Problem
InjuryDec 18, 2025Osseointegration Problem; Osseointegration Problem
INFECTION AND PAIN 3 MONTHS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Pain
MAUDE report 23838562 ↗InjuryNov 21, 2025Osseointegration Problem; Osseointegration Problem
FAILURE 2 DAYS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23623945 ↗InjuryJun 5, 2025Osseointegration Problem; Osseointegration Problem
InjuryJun 2, 2025Loss of Osseointegration; Loss of Osseointegration
INFECTION, GRANULOMA AND BONE LOSS 10 YEARS AFTER IMPLANTATION, PATIENT WITH HYPERTENSION.
Patient problems: Bacterial Infection; Granuloma; Inadequate Osseointegration
MAUDE report 22124087 ↗InjuryMay 15, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
DENTAL IMPLANT FAILURE.
Patient problems: Failure of Implant; Unspecified Infection
MAUDE report 22026029 ↗InjuryApr 29, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY 3 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 21929424 ↗InjuryJan 7, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY 1 MONTH AFTER IMPLANTATION, IMPLANT REMOVED, GRAFTED AND WILL PLACE ANOTHER IMPLANT IN 4 MONTHS.
Patient problems: Inadequate Osseointegration
MAUDE report 21094041 ↗InjurySep 17, 2024Osseointegration Problem; Osseointegration Problem
DENTAL IMPLANT FAILURE.
Patient problems: Failure of Implant; Inadequate Osseointegration
MAUDE report 20234512 ↗
Other Implant, Endosseous, Root-Form devices
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- 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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