Touareg CloseFit™ WP Dental Implant 4.3D 10L ISPX1043Recalls & reported problems
Adin Dental Implant Systems Ltd · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 14
- Deaths reported
- 0
- Injuries reported
- 14
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 14 adverse event reports that list this exact device (DI 07290105152213), received between Feb 6, 2025 and May 13, 2026 — classified as 14 injuries.
The most frequently reported specific device problem is “Osseointegration Problem” (8 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 Problem8
- Patient Device Interaction Problem5
- Loss of Osseointegration1
Patient problems
- Inadequate Osseointegration10
- Bacterial Infection5
- Pain5
- Granuloma1
- Sinus Perforation1
Recent adverse event reports
The 14 most recent of 14 reports, in the reporter's own words as published by the FDA.
InjuryMay 13, 2026Patient Device Interaction Problem
PAIN ONE MONTH AFTER IMPLANTATION. HYPOCHONDRIAC PATIENT.
Patient problems: Pain
MAUDE report 25162754 ↗InjuryJan 5, 2026Patient Device Interaction Problem
PAIN AND MOBILITY 2 WEEKS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration; Pain
MAUDE report 23957883 ↗InjuryAug 26, 2025Osseointegration Problem; Osseointegration Problem
PAIN AND MOBILITY 6 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration; Pain
MAUDE report 22895603 ↗InjuryAug 26, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
MOBILITY 5 DAYS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 22895432 ↗InjuryJul 11, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY AND INFECTION 2 MONTHS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Inadequate Osseointegration
MAUDE report 22485160 ↗InjuryJul 11, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
PAIN, BONE LOSS, SINUS PENETRATION, INFECTION 3 MONTHS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Inadequate Osseointegration; Pain; Sinus Perforation
MAUDE report 22485158 ↗InjuryJun 3, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
PAIN 4 DAYS AFTER IMPLANTATION PATIENT WITH CARDIAC DISEASE.
Patient problems: Pain
MAUDE report 22135807 ↗InjuryFeb 12, 2025Osseointegration Problem; Osseointegration Problem
GRANULOMA, MOBILITY AND INFECTION 1 MONTH AFTER INPLANTATION.
Patient problems: Bacterial Infection; Granuloma; Inadequate Osseointegration
MAUDE report 21364357 ↗InjuryFeb 7, 2025Osseointegration Problem; Osseointegration Problem
INFECTION 4 MONTHS AFTER IMPLANTATION. PATIENT WITH HYPERTENSION AND DIABETES.
Patient problems: Bacterial Infection
MAUDE report 21337313 ↗InjuryFeb 7, 2025Osseointegration Problem; Osseointegration Problem
BONE LOSS FIVE MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 21337308 ↗InjuryFeb 7, 2025Osseointegration Problem; Osseointegration Problem
BONE LOSS 3 MONTH AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 21337305 ↗InjuryFeb 6, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryFeb 6, 2025Osseointegration Problem; Osseointegration Problem
FAILURE 3 MONTH AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 21326952 ↗InjuryFeb 6, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY 3 MONTH AFTER IMPLANTATION, SMOKER.
Patient problems: Inadequate Osseointegration
MAUDE report 21326950 ↗
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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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