Touareg™-S Dental Implant 4.2D 6.25L ISPS0642Recalls & reported problems
Adin Dental Implant Systems Ltd · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 14
- Deaths reported
- 0
- Injuries reported
- 14
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 14 adverse event reports that list this exact device (DI 07290105151728), received between Mar 12, 2025 and Jun 26, 2026 — classified as 14 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
- Loss of Osseointegration3
- Patient Device Interaction Problem3
- Fracture2
Patient problems
- Inadequate Osseointegration12
- Failure of Implant3
- Granuloma1
- Pain1
Recent adverse event reports
The 14 most recent of 14 reports, in the reporter's own words as published by the FDA.
InjuryJun 26, 2026Loss of Osseointegration
MOBILITY4 YEARS AND 4 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 25641345 ↗InjuryMay 18, 2026Loss of Osseointegration
BONE LOSS AND GRANULOMA 6 YEARS AND 3 MONTHS.
Patient problems: Granuloma; Inadequate Osseointegration
MAUDE report 25204492 ↗InjuryMay 1, 2026Patient Device Interaction Problem
MOBILITY 3 WEEKS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 25058003 ↗InjuryMay 1, 2026Osseointegration Problem
MOBILITY 9 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 25058001 ↗InjuryMar 23, 2026Patient Device Interaction Problem
MOBILITY 1 MONTH AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24664729 ↗InjuryJan 20, 2026Patient Device Interaction Problem
MOVILITY 4 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24120914 ↗InjuryJan 14, 2026Fracture
InjuryNov 17, 2025Osseointegration Problem; Osseointegration Problem
PAIN AND MOBILITY 4 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration; Pain
MAUDE report 23569275 ↗InjuryNov 12, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY 2 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23534165 ↗InjuryNov 12, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY 2 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23534160 ↗InjuryNov 6, 2025Loss of Osseointegration; Loss of Osseointegration
MOBILITY 1 YEAR AND 5 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23487383 ↗InjuryNov 6, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY 9 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23487382 ↗InjuryMay 15, 2025Osseointegration Problem; Osseointegration Problem
DENTAL IMPLANT FAILURE
Patient problems: Failure of Implant; Inadequate Osseointegration
MAUDE report 22025958 ↗InjuryMar 12, 2025Fracture; Fracture
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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