Touareg™-S Dental Implant 4.2D 8L ISPS0842Recalls & 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 4.2D 8L dental implant is a screw placed in the jawbone to hold a replacement tooth. The 28 reports mostly describe implants that fail to fuse with the bone, loosen, or break, along with pain and bacterial infection in the weeks or months after placement. All 28 report injuries; no deaths were reported. One report describes the surgical driver cold-welding to the implant so both had to come out together. 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
- 28
- Deaths reported
- 0
- Injuries reported
- 28
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 28 adverse event reports that list this exact device (DI 07290105151773), received between Jul 7, 2024 and Jun 1, 2026 — classified as 28 injuries.
The most frequently reported specific device problem is “Loss of Osseointegration” (10 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
- Loss of Osseointegration10
- Patient Device Interaction Problem9
- Osseointegration Problem6
- Fracture3
Patient problems
- Inadequate Osseointegration20
- Bacterial Infection6
- Failure of Implant4
- Pain3
Recent adverse event reports
The 25 most recent of 28 reports, in the reporter's own words as published by the FDA.
InjuryJun 1, 2026Loss of Osseointegration
MOBILITY 3 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 25350723 ↗InjuryMay 22, 2026Patient Device Interaction Problem
PAIN AND INFECTION 2 MONTHS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Pain
MAUDE report 25256970 ↗InjuryMay 18, 2026Patient Device Interaction Problem
MOBILITY A MONTH AND HALF AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 25204501 ↗InjuryMay 12, 2026Patient Device Interaction Problem
PAIN AND INFECTION 10 DAYS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Pain
MAUDE report 25149252 ↗InjuryMar 23, 2026Patient Device Interaction Problem
MOBILITY ONE MONTH AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24664745 ↗InjuryFeb 10, 2026Osseointegration Problem
DRIVER COLD-WELDED TO THE IMPLANT, THE ONLY POSSIBLE WAY TO REMOVE DRIVER WAS REMOVING IMPLANT AS WELL.
Patient problems: Inadequate Osseointegration
MAUDE report 24305537 ↗InjuryFeb 4, 2026Loss of Osseointegration
MOBILITY 7 YEARS AND 4 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24260613 ↗InjuryFeb 4, 2026Patient Device Interaction Problem
InjuryFeb 4, 2026Osseointegration Problem
MOBILITY ONE YEAR AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24260533 ↗InjuryDec 18, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY AND INFECTION 4 MONTHS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Inadequate Osseointegration
MAUDE report 23838561 ↗InjuryDec 17, 2025Loss of Osseointegration; Loss of Osseointegration
MOBILITY 5 YEARS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23830297 ↗InjuryDec 8, 2025Fracture; Fracture
InjuryDec 8, 2025Fracture; Fracture
InjuryNov 6, 2025Loss of Osseointegration; Loss of Osseointegration
MOBILITY 11 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23487384 ↗InjuryAug 20, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY ONE MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 22854371 ↗InjuryJul 28, 2025Loss of Osseointegration; Loss of Osseointegration
MOBILITY 3 YEARS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 22634015 ↗InjuryJul 14, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryJun 12, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
MOBILITY A MONTH AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 22195652 ↗InjuryJun 6, 2025Loss of Osseointegration; Loss of Osseointegration
MOBILITY 2 YEARS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 22161443 ↗InjuryJun 6, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryJun 2, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY 3 MONTH AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 22124488 ↗InjuryMay 21, 2025Loss of Osseointegration; Loss of Osseointegration
MOBILITY 4 YEARS AFTER IMPLANTATION, PATIENT WITH CANCER, HYPERTENSION, KIDNEY DISEASE AND ARTHRITIS CURRENCTLY RECEIVING CHEMOTHERAPY AND RADIOTHERAPY.
Patient problems: Inadequate Osseointegration
MAUDE report 22062604 ↗InjuryMay 15, 2025Osseointegration Problem; Osseointegration Problem
DENTAL IMPLANT FAILURE.
Patient problems: Failure of Implant; Inadequate Osseointegration
MAUDE report 22025797 ↗InjuryApr 29, 2025Loss of Osseointegration; Loss of Osseointegration
MOBILITY 7 YEARS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 21929366 ↗InjuryMar 21, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
PAIN AND MOBILITY 3 WEEKS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration; Pain
MAUDE report 21664240 ↗
Other Implant, Endosseous, Root-Form devices
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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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