Touareg CloseFit™ WP Dental Implant 4.3D 11.5L ISPX1143Recalls & reported problems
Adin Dental Implant Systems Ltd · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 12
- Deaths reported
- 0
- Injuries reported
- 12
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 12 adverse event reports that list this exact device (DI 07290105152275), received between Sep 17, 2024 and May 13, 2026 — classified as 12 injuries.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (9 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 Problem9
- Osseointegration Problem3
Patient problems
- Inadequate Osseointegration10
- Failure of Implant2
- Bacterial Infection1
- Pain1
Recent adverse event reports
The 12 most recent of 12 reports, in the reporter's own words as published by the FDA.
InjuryMay 13, 2026Osseointegration Problem
MOBILITY AND BONE LOSS ONE MONTH AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 25162763 ↗InjuryApr 16, 2026Patient Device Interaction Problem
MOBILITY 4 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24904899 ↗InjuryMar 23, 2026Patient Device Interaction Problem
MOBILITY 1 MONTHS AFTER IMPLANTATION. PATIENT WITH HYPERTENSION.
Patient problems: Inadequate Osseointegration
MAUDE report 24664770 ↗InjuryAug 20, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
PAIN 2 DAYS AFTER IMPLANTATION, PATIENT WITH HYPERTENSION.
Patient problems: Pain
MAUDE report 22854351 ↗InjuryJul 11, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
MOBILITY 3 MONTHS AFTER IMPLANTATION. PATIENT WITH CARDIAC PROBLEMS.
Patient problems: Inadequate Osseointegration
MAUDE report 22485188 ↗InjuryJul 11, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
MOBILITY 4 MONTHS AFTER IMPLANTATION. SMOKER PATIENT.
Patient problems: Inadequate Osseointegration
MAUDE report 22485178 ↗InjuryJul 11, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
MOBILITY A WEEK AFTER IMPLANTATION. SMOKER PATIENT.
Patient problems: Inadequate Osseointegration
MAUDE report 22485177 ↗InjuryJul 11, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
MOBILITY 2 MONTH AFTER IMPLANTATION, SMOKER AND CANCER PATIENT.
Patient problems: Inadequate Osseointegration
MAUDE report 22485176 ↗InjuryJul 11, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryJun 18, 2025Osseointegration Problem; Osseointegration Problem
DENTAL IMPLANT FAILURE.
Patient problems: Failure of Implant; Inadequate Osseointegration
MAUDE report 22283089 ↗InjuryMar 6, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
MOBILITY 4 DAYS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 21539993 ↗InjurySep 17, 2024Osseointegration Problem; Osseointegration Problem
DENTAL IMPLANT FAILURE.
Patient problems: Failure of Implant; Inadequate Osseointegration
MAUDE report 20234511 ↗
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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