Touareg™-S Dental Implant 4.2D 11.5L ISPS1142Recalls & reported problems
Adin Dental Implant Systems Ltd · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 25
- Deaths reported
- 0
- Injuries reported
- 25
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 25 adverse event reports that list this exact device (DI 07290105151872), received between Dec 7, 2022 and Sep 10, 2026 — classified as 25 injuries.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (11 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
- Patient Device Interaction Problem11
- Osseointegration Problem10
- Loss of Osseointegration4
- Failure to Osseointegrate2
- Fracture2
Patient problems
- Inadequate Osseointegration8
- Pain8
- Bacterial Infection7
- Failure of Implant6
- Granuloma1
- Implant Pain1
- Nerve Damage1
- Osteolysis1
Recent adverse event reports
The 25 most recent of 25 reports, in the reporter's own words as published by the FDA.
InjurySep 10, 2026Osseointegration Problem
InjurySep 10, 2026Failure to Osseointegrate; Osseointegration Problem
Dental implant failure.
Patient problems: Failure of Implant; Inadequate Osseointegration
MAUDE report 50712565 ↗InjurySep 6, 2026Osseointegration Problem; Patient Device Interaction Problem
Patient problems: Failure of Implant; Unspecified Infection
MAUDE report 50637920 ↗InjuryJun 29, 2026Osseointegration Problem
INFECTION, PAIN 14 DAYS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Pain
MAUDE report 25654424 ↗InjuryMay 28, 2026Loss of Osseointegration
MOBILITY 9 YEARS AND 6 MONTHS AFTER IMPLANTATION. PATIENT WITH ASTHMA.
Patient problems: Bacterial Infection; Inadequate Osseointegration
MAUDE report 25318408 ↗InjuryMar 23, 2026Patient Device Interaction Problem
MOBILITY 1 WEEK AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24664751 ↗InjuryFeb 10, 2026Osseointegration Problem
INFECTION 3 MONTHS AFTER IMPLANTATION. DIABETIC PATIENT.
Patient problems: Bacterial Infection
MAUDE report 24305574 ↗InjuryFeb 10, 2026Patient Device Interaction Problem
InjuryFeb 4, 2026Patient Device Interaction Problem
InjuryFeb 3, 2026Patient Device Interaction Problem
NERVE IMPACTATION ONE MONTH AFTER IMPLANTATION. ALCOHOLIC AND HYPERTENSION.
Patient problems: Nerve Damage
MAUDE report 24246808 ↗InjuryFeb 3, 2026Patient Device Interaction Problem
InjuryDec 8, 2025Fracture; Fracture
InjuryNov 3, 2025Fracture; Fracture
InjuryOct 15, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY 7 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23284952 ↗InjurySep 17, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
InjurySep 17, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryAug 4, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryAug 4, 2025Loss of Osseointegration; Loss of Osseointegration
PAIN AND INFECTION 11 MONTHS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Pain
MAUDE report 22705839 ↗InjuryJul 28, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY 5 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 22633667 ↗InjuryJun 18, 2025Osseointegration Problem; Osseointegration Problem
DENTAL IMPLANT FAILURE.
Patient problems: Failure of Implant; Inadequate Osseointegration
MAUDE report 22283082 ↗InjuryJun 6, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryJun 2, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryMar 18, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY 3 MONTH AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 21631883 ↗InjuryJan 7, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
INFECTION A MONTH AFTER IMPLANTATION. IMPLANT REMOVED. DIABETIC PATIENT.
Patient problems: Bacterial Infection
MAUDE report 21094055 ↗InjuryDec 7, 2022Failure to Osseointegrate; Loss of Osseointegration; Osseointegration Problem; Failure to Osseointegrate; Loss of Osseointegration; Osseointegration Problem
FAILED DENTAL IMPLANT, PATIENT REPORTED PAIN AND MOBILITY.
Patient problems: Inadequate Osseointegration; Osteolysis; Pain
MAUDE report 15930507 ↗
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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