Touareg™-S Dental Implant 5.0D 10L ISPS1050Recalls & 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 dental implant is a screw-shaped tooth root used to anchor a replacement tooth in the jaw. The 37 reports to FDA describe implants that fail to fuse properly with the bone, leaving them loose with pain, bone loss, and infection around the implant site, sometimes within weeks of placement and sometimes years later. All 37 reports describe injuries, with no deaths. 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
- 38
- Deaths reported
- 0
- Injuries reported
- 38
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 38 adverse event reports that list this exact device (DI 07290105151834), received between Jan 7, 2025 and Sep 6, 2026 — classified as 38 injuries.
The most frequently reported specific device problem is “Osseointegration 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
- Osseointegration Problem18
- Patient Device Interaction Problem15
- Loss of Osseointegration5
- Failure to Osseointegrate2
Patient problems
- Inadequate Osseointegration20
- Bacterial Infection14
- Pain14
- Failure of Implant4
- Unspecified Infection2
Recent adverse event reports
The 25 most recent of 38 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 50637915 ↗InjuryJul 10, 2026Loss of Osseointegration
PAIN AND BONE LOSS 3 YEARS AND 9 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration; Pain
MAUDE report 25786745 ↗InjuryJun 26, 2026Osseointegration Problem
MOBILITY AND BONE LOSS 2 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 25641336 ↗InjuryMay 22, 2026Osseointegration Problem
InjuryMay 12, 2026Osseointegration Problem
InjuryApr 7, 2026Osseointegration Problem
MOBILITY THREE AND HALF MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24807781 ↗InjuryMar 23, 2026Osseointegration Problem
PAIN AND INFECTION 2 WEEKS AFTER IMPLANTATIONS.
Patient problems: Bacterial Infection; Pain
MAUDE report 24664749 ↗InjuryFeb 16, 2026Osseointegration Problem
INFECTION, MOBILITY, PAIN 5 MONTH AFTER IMPLANTATION. PATIENT WITH HYPERTENSION, PROSTATE CANCER AND STAGE 3 KIDNEY DISEASE.
Patient problems: Bacterial Infection; Inadequate Osseointegration; Pain
MAUDE report 24345321 ↗InjuryFeb 16, 2026Patient Device Interaction Problem
BONE LOSS 2 YEARS AFTER IMPLANTATION, PATIENT WITH HYPERTENSION, GLAUCOMA AND BENIGN PROSTATIC HYPERPLASIA.
Patient problems: Inadequate Osseointegration
MAUDE report 24345319 ↗InjuryFeb 10, 2026Osseointegration Problem
InjuryFeb 10, 2026Patient Device Interaction Problem
InjuryFeb 3, 2026Patient Device Interaction Problem
PAIN AND INFECTION ONE MONTH AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Pain
MAUDE report 24246858 ↗InjuryNov 25, 2025Osseointegration Problem; Osseointegration Problem
InjuryNov 25, 2025Osseointegration Problem; Osseointegration Problem
PAIN AND INFECTION 2 MONTHS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Pain
MAUDE report 23650066 ↗InjuryNov 21, 2025Osseointegration Problem; Osseointegration Problem
PAIN AND MOBILITY 4 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration; Pain
MAUDE report 23622483 ↗InjuryNov 21, 2025Osseointegration Problem; Osseointegration Problem
PAIN AND MOBILITY 5 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration; Pain
MAUDE report 23622482 ↗InjuryNov 17, 2025Osseointegration Problem; Osseointegration Problem
BUCCAL BONE LOSS 9 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23569271 ↗InjuryNov 12, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
MOBILITY ONE MONTH AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23534151 ↗InjuryNov 12, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
MOBILITY 1 MONTH AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23534144 ↗InjuryNov 11, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
MOBILIYY 2 MONTH AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23525617 ↗InjuryNov 11, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY 1 MONTH AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23525605 ↗InjuryNov 11, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY A MONTH AFTE IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23525604 ↗InjuryOct 15, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryOct 15, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
InjurySep 19, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY 2 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23095486 ↗
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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