3i T3® DCD® BNET410Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00844868033059), received between Nov 5, 2020 and Sep 16, 2022 — classified as 3 injuries.

The most frequently reported specific device problem is “Mechanical Problem” (1 report).

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 16, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjurySep 16, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED PERI-IMPLANTITIS WITH INFLAMMATION, PUS.

  Patient problems: Inflammation; Osteolysis; Unspecified Infection

  MAUDE report 15436194 ↗
• InjuryJun 17, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH #45 WAS REMOVED DUE TO PERI-IMPLANTITIS. ABSCESS WAS REPORTED AS A RESULT OF THE EVENT.

  Patient problems: Abscess; Osteolysis; Unspecified Infection

  MAUDE report 12021268 ↗
• InjuryNov 5, 2020Mechanical Problem; Mechanical Problem

  DOCTOR REPORTED THAT WHEN THE DOCTOR WAS PLACING THE IMPLANT, THE MOUNT DOES NOT DISENGAGED FROM THE IMPLANT. DOCTOR DID NOT FINISHED THE PROCEDURE AND PATIENT WILL HAVE TO RETURN FOR THE IMPLANT PLACEMENT IN A LATER POINT OF TIME.

  Patient problems: No Information

  MAUDE report 10790598 ↗