3i T3® DCD® BNST3213Recalls & reported problems

Summary

The FDA's MAUDE database contains 25 adverse event reports that list this exact device (DI 00844868029113), received between Sep 3, 2019 and Apr 16, 2026 — classified as 25 injuries.

The most frequently reported specific device problem is “Fracture” (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 25 most recent of 25 reports, in the reporter's own words as published by the FDA.

• InjuryApr 16, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #12 WAS REMOVED DUE TO PERI-IMPLANTITIS. FAILED IST DURING UNCOVERING PROCEDURE AND WAS REMOVED.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 24896740 ↗
• InjuryApr 7, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT IMPLANT WAS REMOVED DUE TO BONE LOSS. PATIENT PRESENTED WITH BONE LOSS ON THE BUCCAL/CORONAL PORTION AT TIME OF PHASE 2 IMPLANT RECOVERY. IMPLANT 10 REMOVED AND GRAFTED BONE RESTORATION WAS COMPLETED IN ORDER TO PLACE NEW IMPLANTS IN FUTURE. NOTED INFLAMMATION.

  Patient problems: Inflammation; Osteolysis

  MAUDE report 24809191 ↗
• InjuryApr 7, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT IMPLANT WAS REMOVED DUE TO BONE LOSS. PATIENT PRESENTED WITH BONE LOSS ON THE BUCCAL/CORONAL PORTION AT TIME OF PHASE 2 IMPLANT RECOVERY. IMPLANT 7 REMOVED AND GRAFTED BONE RESTORATION WAS COMPLETED IN ORDER TO PLACE NEW IMPLANTS IN FUTURE. NOTED INFLAMMATION.

  Patient problems: Inflammation; Osteolysis

  MAUDE report 24809187 ↗
• InjuryOct 4, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT HAD PAIN AND GRANULOMA OVER THE IMPLANT AT TOOTH LOCATION #26, WITH PURULENCE EMANATING FROM THE GRANULOMA. THE IMPLANT WAS REMOVED DUE TO PERI-IMPLANTITIS. SYMPTOMS AS A RESULT OF THE EVENT: INFLAMMATION.

  Patient problems: Inflammation; Osteolysis; Unspecified Infection

  MAUDE report 20371809 ↗
• InjurySep 18, 2024Adverse 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 POSITIONS NUMBER #22 & #23 FAILED DUE TO PERI-IMPLANTITIS AND WERE REMOVED. THE PROCEDURE WAS NOT CONCLUDED BY PLACING ANOTHER IMPLANTS.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 20244986 ↗
• InjuryJun 11, 2024Adverse 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 POSITIONS NUMBER 32 & 43 FAILED DUE TO PERI-IMPLANTITIS. THE DOCTOR REPORTS THAT THE PROCEDURE WAS NOT CONCLUDED BY PLACING ANOTHER IMPLANTS. THE DOCTOR ALSO REPORTED INFLAMMATION, PAIN, EDEMA AND ABSCESS.

  Patient problems: Osteolysis; Pain; Unspecified Infection

  MAUDE report 19508237 ↗
• InjuryJun 5, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE DOCTOR REPORTS THAT THE DENTAL IMPLANT LOCATED IN DENTAL POSITION NUMBER #12 FAILED DUE TO PERI-IMPLANTITIS. THE DOCTOR REPORTS THAT THE PROCEDURE WAS NOT CONCLUDED BY PLACING ANOTHER IMPLANT. BONE TYPE: III

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 19465833 ↗
• InjuryMay 24, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT WAS REMOVED DUE TO PERI-IMPLANTITIS. TOOTH SITE 11, AT TORQUE TEST IMPLANT COME OUT. SITE WAS DEBRIDED.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 19392520 ↗
• InjuryMay 23, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT WAS REMOVED DUE TO BONE LOSS AND INFECTION. TOOTH #24. SYMPTOMS AS A RESULT OF THE EVENT: PAIN AND INFLAMMATION.

  Patient problems: Osteolysis; Pain; Unspecified Infection

  MAUDE report 19383349 ↗
• InjuryFeb 28, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED, THAT THE PATIENT EXPERIENCED BONE LOSS. AND INFECTION AT IMPLANT TOOTH SITES #23 AND 26, WITH ASSOCIATED ABSCESS. THEREFORE, THE IMPLANTS WERE REMOVED.

  Patient problems: Erosion; Osteolysis; Unspecified Infection

  MAUDE report 18804639 ↗
• InjuryOct 26, 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 DENTAL POSITION NUMBER #32 FAILED DUE TO PERI-IMPLANTITIS. THE DOCTOR REPORTS IN THE PER THAT THE PROCEDURE WAS NOT CONCLUDED BY PLACING ANOTHER IMPLANT.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 18016672 ↗
• InjuryOct 13, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT EXPERIENCED BONE LOSS AND INFECTION AT IMPLANT TOOTH SITES #23 AND 26, WITH ASSOCIATED ABSCESS. THEREFORE, THE IMPLANTS WERE REMOVED.

  Patient problems: Erosion; Osteolysis; Unspecified Infection

  MAUDE report 17935533 ↗
• InjuryOct 13, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  BONE LOSS AROUND THE IMPLANT. BONE GRAFT SITE AFTER REMOVAL OF IMPLANT. TOOTH #6.

  Patient problems: Osteolysis

  MAUDE report 17932171 ↗
• InjurySep 18, 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 POSITIONS NUMBER #24 AND #25 FAILED DUE TO PERI-IMPLANTITIS. THE PROCEDURE WAS NOT CONCLUDED BY PLACING ANOTHER IMPLANTS.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 17764457 ↗
• InjuryJul 13, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE DENTAL IMPLANT LOCATED IN DENTAL POSITION NUMBER #23 FAILED AND WAS REMOVED DUE TO PERI-IMPLANTITIS. SYMPTOM AS A RESULT OF EVENT: ABSCESS.

  Patient problems: Erosion; Osteolysis; Unspecified Infection

  MAUDE report 17321519 ↗
• InjuryJun 28, 2023Fracture; Fracture

  NO ADDITIONAL EVENT INFORMATION RECEIVED AT THE TIME OF THIS REPORT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17219294 ↗
• InjuryApr 12, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE 12 WAS REMOVED DUE TO PERI-IMPLANTITIS. IMPLANT WAS PLACED WITH GOOD PRIMARY STABILITY. SURGICAL INTERVENTION WAS NEEDED TO AVOID BONE LOSS. PATIENT WILL HAVE TO RETURN TO PLACE A NEW IMPLANT.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 16726270 ↗
• InjuryMar 17, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Inflammation; Pain; Unspecified Infection

  MAUDE report 16564345 ↗
• InjuryMar 8, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH LOCATION #26 WAS REMOVED DUE TO INFECTION. SYMPTOMS AS A RESULT OF THE EVENT: PAIN, INFLAMMATION.

  Patient problems: Inflammation; Pain; Unspecified Infection

  MAUDE report 16504052 ↗
• InjuryJun 20, 2022Adverse 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 #22 FAILED DUE TO PERI-IMPLANTITIS. THE DOCTOR CONFIRMS THAT THE PATIENT MUST RETURN IN THE FUTURE TO COMPLETE THE SURGICAL PROCEDURE. THE DOCTOR REPORTS THAT THE PATIENT DID NOT SUFFER ANY INCONVENIENCE OR ANY MAJOR IMPACT ON HIS HEALTH AS A RESULT OF THE EVENT.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 14741673 ↗
• InjuryNov 10, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO ADDITIONAL EVENT INFORMATION AT THE TIME OF THIS REPORT.

  Patient problems: Abscess; Osteolysis; Pain; Unspecified Infection

  MAUDE report 12790824 ↗
• InjuryOct 19, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  DOCTOR REPORTS THAT THE BNST3213 IMPLANT WAS REMOVED DUE TO PERI-IMPLANTITIS. TOOTH SITE 5.

  Patient problems: No Code Available; Unspecified Infection

  MAUDE report 10698905 ↗
• InjurySep 7, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED IMPLANT WAS PLACED AND REMOVED DURING THE SAME SURGERY DUE TO LACK OF PRIMARY STABILITY. NO OTHER IMPLANT WAS PLACED DURING THE SAME SURGERY.

  Patient problems: No Information

  MAUDE report 10498699 ↗
• InjurySep 3, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE DOCTOR WAS UNABLE TO PLACE THE IMPLANT INTO THE PATIENT'S OSTEOTOMY.

  Patient problems: No Code Available

  MAUDE report 8955645 ↗
• InjurySep 3, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE DOCTOR WAS UNABLE TO PLACE THE IMPLANT INTO THE PATIENT'S OSTEOTOMY.

  Patient problems: No Code Available

  MAUDE report 8955521 ↗