Touareg™-S Dental Implant 3.75D 11.5L ISPS1138Recalls & reported problems
Adin Dental Implant Systems Ltd · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This ADIN Dental Touareg-S endosseous dental implant is a root-form screw placed into the jawbone. The 33 reports mostly describe implants that fail to fuse properly with bone or lose that fusion later, often becoming loose or mobile within months, sometimes years, after placement, along with infection, pain, and sinus problems. All 33 reports involve injuries, and no deaths are described. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 32
- Deaths reported
- 0
- Injuries reported
- 32
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 32 adverse event reports that list this exact device (DI 07290105151865), received between Oct 9, 2023 and May 22, 2026 — classified as 32 injuries.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (18 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 Problem18
- Osseointegration Problem8
- Fracture3
- Loss of Osseointegration3
- Separation Failure1
Patient problems
- Inadequate Osseointegration15
- Bacterial Infection8
- Pain8
- Failure of Implant6
- Sinus Perforation2
- Unspecified Infection2
Recent adverse event reports
The 25 most recent of 32 reports, in the reporter's own words as published by the FDA.
InjuryMay 22, 2026Osseointegration Problem
InjuryMay 12, 2026Patient Device Interaction Problem
PAIN AND INFECTION 1 MONTH AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Pain
MAUDE report 25149259 ↗InjuryMay 1, 2026Loss of Osseointegration
InjuryMar 23, 2026Patient Device Interaction Problem
MOBILITY ONE MONTH AND HALF AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24664761 ↗InjuryFeb 10, 2026Patient Device Interaction Problem
SINUS PENETRATION, 3 YEARS AFTER IMPLANTATION.
Patient problems: Sinus Perforation
MAUDE report 24307363 ↗InjuryFeb 4, 2026Osseointegration Problem
MOBILITY 2 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24260577 ↗InjuryFeb 4, 2026Osseointegration Problem
MOBILITY 2 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24260576 ↗InjuryFeb 2, 2026Patient Device Interaction Problem
PAIN AND MOBILITY 2 WEEKS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration; Pain
MAUDE report 24240357 ↗InjuryFeb 2, 2026Patient Device Interaction Problem
INFECTION AND SINUS PENETRATION 2 WEEKS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Sinus Perforation
MAUDE report 24240356 ↗InjuryJan 20, 2026Patient Device Interaction Problem
MOBILITY 2 WEEKS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24120525 ↗InjuryJan 12, 2026Osseointegration Problem
MOBILITY 5 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24036213 ↗InjuryNov 21, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY 3 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23622499 ↗InjuryNov 12, 2025Osseointegration Problem; Osseointegration Problem
PAIN A WEEK AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration; Pain
MAUDE report 23534140 ↗InjuryOct 15, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
MOBILITY ONE WEEK AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23285016 ↗InjuryOct 15, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
InjurySep 19, 2025Loss of Osseointegration; Loss of Osseointegration
PAIN AND MOBILITY 3 YEARS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration; Pain
MAUDE report 23095485 ↗InjurySep 17, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryAug 20, 2025Osseointegration Problem; Osseointegration Problem
InjuryAug 20, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
PAIN AND INFECTION 3 MONTHS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Pain
MAUDE report 22854369 ↗InjuryAug 20, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
PAIN AND INFECTION 20 DAYS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Pain
MAUDE report 22854367 ↗InjuryAug 20, 2025Osseointegration Problem; Osseointegration Problem
InjuryJul 31, 2025Fracture; Fracture
InjuryJun 6, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
MOBILITY ONE MONTH AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 22161450 ↗InjuryJun 6, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
MOBILITY 3 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 22161442 ↗InjuryJun 2, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
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.
How reports and recalls are matched · Editorial policy · Report an error on this page