Touareg™-S Dental Implant 3.75D 10L ISPS1038Recalls & 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 root implant placed into the jawbone to hold a tooth replacement. The 37 reports mostly describe implants that fail to bond with the bone, so the implant becomes loose or is lost, along with infection, pain, and occasional fracture. No deaths were reported and all 37 reports involved injuries. There are no recalls naming this device. Reports rose from 9 in the earlier12-month period to 26 in the most recent.
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 07290105151810), received between Jul 7, 2024 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
- Loss of Osseointegration9
- Patient Device Interaction Problem9
- Fracture4
Patient problems
- Inadequate Osseointegration27
- Bacterial Infection8
- Failure of Implant7
- Pain4
- Unspecified Infection2
- Osteolysis1
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 50637921 ↗InjurySep 6, 2026Osseointegration Problem; Patient Device Interaction Problem
Patient problems: Failure of Implant; Unspecified Infection
MAUDE report 50637907 ↗InjuryJun 26, 2026Osseointegration Problem
MOBILITY 4 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 25641346 ↗InjuryJun 1, 2026Patient Device Interaction Problem
MOBILITY 1 MONTH AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 25354898 ↗InjuryMay 28, 2026Osseointegration Problem
MOBILITY 1 MONTH AFTER IMPLANTATION. DIABETIC AND ASTHMA PATIENT.
Patient problems: Inadequate Osseointegration
MAUDE report 25318405 ↗InjuryMay 22, 2026Patient Device Interaction Problem
InjuryMay 12, 2026Osseointegration Problem
PAIN AND INFECTION 3 YEARS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Pain
MAUDE report 25149255 ↗InjuryMay 12, 2026Patient Device Interaction Problem
InjuryMay 1, 2026Loss of Osseointegration
MOBILITY 4 YEARS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 25057995 ↗InjuryApr 28, 2026Loss of Osseointegration
MOBILITY AND BONE LOSS 2 YEARS AND 2 MONTHS AFTER IMPLANTATIO. PATIENT WITH PACEMAKER, ANEURYSM AND HYPERTENSION.
Patient problems: Inadequate Osseointegration
MAUDE report 25020805 ↗InjuryApr 7, 2026Patient Device Interaction Problem
MOBILITY ONE MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24807993 ↗InjuryMar 23, 2026Loss of Osseointegration
MOBILITY AND BONE LOSS 6 YEARS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24664767 ↗InjuryFeb 10, 2026Osseointegration Problem
BONE LOSS AND INFECTION 4 MONTHS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Inadequate Osseointegration
MAUDE report 24305577 ↗InjuryFeb 10, 2026Osseointegration Problem
MOBILITY 7 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24305535 ↗InjuryFeb 4, 2026Patient Device Interaction Problem
MOBILITY 10 DAYS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24260614 ↗InjuryFeb 4, 2026Osseointegration Problem
InjuryJan 26, 2026Patient Device Interaction Problem
MOBILITY ONE MONTH AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24181805 ↗InjuryDec 18, 2025Fracture; Fracture
InjuryDec 17, 2025Loss of Osseointegration; Loss of Osseointegration
MOBILITY AND PAIN 3 YEARS AND 3 MONTH AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration; Pain
MAUDE report 23829193 ↗InjuryNov 21, 2025Osseointegration Problem; Osseointegration Problem
PAIN, MOBILITY AND INFECTION 4 MONTHS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Inadequate Osseointegration; Pain
MAUDE report 23622454 ↗InjuryNov 17, 2025Fracture; Fracture
IMPLANT FRACTURE 4 YEARS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23569270 ↗InjuryNov 12, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY ONE MONTH AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23534145 ↗InjuryNov 12, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
MOBILITY 21 DAYS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23534138 ↗InjuryNov 6, 2025Loss of Osseointegration; Loss of Osseointegration
MOBILITY 2 YEARS AND 6 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23487415 ↗InjuryNov 6, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY 11 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23487394 ↗
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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