3i T3® DCD® BNET411Recalls & reported problems

Summary

The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00844868033066), received between Sep 7, 2020 and Jul 8, 2024 — classified as 9 injuries.

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 9 most recent of 9 reports, in the reporter's own words as published by the FDA.

• InjuryJul 8, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT IS REPORTED THAT THE IMPLANT IN TOOTH SITE #46 WAS REMOVED DUE TO PERIIMPLANTITIS. ADDITIONAL APPOINTMENT REQUIRED: NO. SYMPTOMS AS A RESULT OF THE EVENT: NO PATIENT IMPACT.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 19687812 ↗
• InjuryFeb 1, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  8 WEEKS AFTER IMPLANT PLACEMENT, X-RAY SHOWED RADIOLUCENCY AROUND APICAL 1/2 OF UNLOADED IMPLANT. IT WAS REMOVED ALONG WITH GRANULATION TISSUE. TOOTH #10.

  Patient problems: Unspecified Infection

  MAUDE report 18622697 ↗
• InjurySep 19, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE DOCTOR REPORTS THAT THE DENTAL IMPLANTS LOCATED IN DENTAL POSITION NUMBER #32, #42 AND #43 FAILED DUE TO PERI-IMPLANTITIS. THE PROCEDURE WAS NOT CONCLUDED BY PLACING ANOTHER IMPLANTS. SITES PRESENTED INFLAMMATION AND EDEMA. PATIENT FELT PAIN.

  Patient problems: Osteolysis; Pain; Unspecified Infection

  MAUDE report 17771538 ↗
• InjuryJan 20, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE DOCTOR REPORTS THAT THE DENTAL IMPLANT LOCATED IN POSITION NUMBER #25 FAILED DUE TO PERI-IMPLANTITIS. THE DOCTOR REPORTS INFLAMMATION. THE DOCTOR MENTIONS IN THE PER FORM THAT THE PROCEDURE WAS COMPLETED WITH ANOTHER IMPLANT IN THAT SURGERY.

  Patient problems: Inflammation; Osteolysis; Unspecified Infection

  MAUDE report 16218838 ↗
• InjuryJan 20, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE DOCTOR REPORTS THAT THE DENTAL IMPLANT LOCATED IN POSITION NUMBER #26 FAILED DUE TO PERI-IMPLANTITIS. THE DOCTOR REPORTS INFLAMMATION. THE DOCTOR MENTIONS IN THE PER FORM THAT THE PROCEDURE WAS NOT COMPLETED WITH ANOTHER IMPLANT IN THAT SURGERY.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 16218663 ↗
• InjuryJul 21, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE DENTAL IMPLANT LOCATED IN POSITIONS NUMBER # 22 FAILED DUE TO INFECTION. THE DOCTOR CONFIRMS THAT THE PROCEDURE WAS NOT COMPLETED WITH ANOTHER IMPLANT. THE DOCTOR REPORTED: INFLAMMATION.

  Patient problems: Inflammation; Unspecified Infection

  MAUDE report 15074230 ↗
• InjuryFeb 8, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE 8 LACKED PRIMARY STABILITY WHEN PLACING AND WAS REMOVED, PROCEDURE WAS NOT COMPLETED WITH ANOTHER IMPLANT.

  Patient problems: No Information

  MAUDE report 11292316 ↗
• InjuryNov 5, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  DOCTOR REPORTED THE IMPLANT IN TOOTH LOCATION 19 WAS REMOVED DUE TO INFECTION. SITE PRESENTED INFLAMMATION.

  Patient problems: Inflammation; Unspecified Infection

  MAUDE report 10790913 ↗
• InjurySep 7, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED IMPLANT PLACED AND REMOVED DURING THE SAME SURGERY DUE TO LACK OF PRIMARY STABILITY. ANOTHER IMPLANT WAS PLACED ONE MONTH LATER.

  Patient problems: No Code Available

  MAUDE report 10498836 ↗