3i T3 DCDRecalls & reported problems across all models
ZimVie US Corp LLC · 73 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 789
- Deaths reported
- 0
- Injuries reported
- 763
- Recalls
- 0
We found 73 models of 3i T3 DCD by ZimVie US Corp LLC in the FDA's device registry (GUDID). Together they are named in 789 adverse event reports in the FDA's MAUDE database, received between May 29, 2019 and Sep 29, 2026 — classified as 763 injuries, 26 malfunctions.
The most frequently reported specific device problem is “Mechanical Problem” (24 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported 3i T3 DCD problems
Device problems
- Adverse Event Without Identified Device or Use Problem733
- Mechanical Problem24
- Fracture14
- Patient-Device Incompatibility8
- Separation Failure6
- Loss of Osseointegration3
- Detachment of Device or Device Component1
- Difficult to Insert1
Patient problems
- Unspecified Infection550
- Osteolysis392
- Pain185
- Inflammation145
- No Clinical Signs, Symptoms or Conditions73
- Swelling/ Edema61
- No Information47
- No Code Available39
3i T3 DCD models
73 models, most reported first. Each model has its own page with its reports, recalls and device details.
- 3i T3® DCD® BNPT4311IMPLANT, ENDOSSEOUS, ROOT-FORM59 reports
- 3i T3® DCD® BNPT5411IMPLANT, ENDOSSEOUS, ROOT-FORM49 reports
- 3i T3® DCD® BNPT5410IMPLANT, ENDOSSEOUS, ROOT-FORM48 reports
- 3i T3® DCD® BNST3211IMPLANT, ENDOSSEOUS, ROOT-FORM48 reports
- 3i T3® DCD® BNST410IMPLANT, ENDOSSEOUS, ROOT-FORM48 reports
- 3i T3® DCD® BNPT4310IMPLANT, ENDOSSEOUS, ROOT-FORM42 reports
- 3i T3® DCD® BNST3210IMPLANT, ENDOSSEOUS, ROOT-FORM39 reports
- 3i T3® DCD® BNSS410IMPLANT, ENDOSSEOUS, ROOT-FORM28 reports
- 3i T3® DCD® BNPT4313IMPLANT, ENDOSSEOUS, ROOT-FORM27 reports
- 3i T3® DCD® BNPT6510IMPLANT, ENDOSSEOUS, ROOT-FORM26 reports
- 3i T3® DCD® BNST3213IMPLANT, ENDOSSEOUS, ROOT-FORM25 reports
- 3i T3® DCD® BNST411IMPLANT, ENDOSSEOUS, ROOT-FORM25 reports
- 3i T3® DCD® BNST413IMPLANT, ENDOSSEOUS, ROOT-FORM25 reports
- 3i T3® DCD® BNST3285IMPLANT, ENDOSSEOUS, ROOT-FORM23 reports
- 3i T3® DCD® BNPT5485IMPLANT, ENDOSSEOUS, ROOT-FORM20 reports
- 3i T3® DCD® BNPT4385IMPLANT, ENDOSSEOUS, ROOT-FORM19 reports
- 3i T3® DCD® BNST510IMPLANT, ENDOSSEOUS, ROOT-FORM16 reports
- 3i T3® DCD® BNST3215IMPLANT, ENDOSSEOUS, ROOT-FORM13 reports
- 3i T3® DCD® BNST485IMPLANT, ENDOSSEOUS, ROOT-FORM13 reports
- 3i T3® DCD® BNSS510IMPLANT, ENDOSSEOUS, ROOT-FORM13 reports
- 3i T3® DCD® BNST585IMPLANT, ENDOSSEOUS, ROOT-FORM13 reports
- 3i T3® DCD® BNST511IMPLANT, ENDOSSEOUS, ROOT-FORM11 reports
- 3i T3® DCD® BNST415IMPLANT, ENDOSSEOUS, ROOT-FORM10 reports
- 3i T3® DCD® BNPT5413IMPLANT, ENDOSSEOUS, ROOT-FORM10 reports
- 3i T3® DCD® BNSS411IMPLANT, ENDOSSEOUS, ROOT-FORM9 reports
- 3i T3® DCD® BNPT6513IMPLANT, ENDOSSEOUS, ROOT-FORM9 reports
- 3i T3® DCD® BNET411IMPLANT, ENDOSSEOUS, ROOT-FORM9 reports
- 3i T3® DCD® BNPT6511IMPLANT, ENDOSSEOUS, ROOT-FORM6 reports
- 3i T3® DCD® BNSS413IMPLANT, ENDOSSEOUS, ROOT-FORM5 reports
- 3i T3® DCD® BNES465IMPLANT, ENDOSSEOUS, ROOT-FORM5 reports
- 3i T3® DCD® BNES565IMPLANT, ENDOSSEOUS, ROOT-FORM5 reports
- 3i T3® DCD® BNET510IMPLANT, ENDOSSEOUS, ROOT-FORM5 reports
- 3i T3® DCD® BNPS5410IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- 3i T3® DCD® BNPT4315IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- 3i T3® DCD® BNPT5415IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- 3i T3® DCD® BNET415IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- 3i T3® DCD® BNET585IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- 3i T3® DCD® BNSS311IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- 3i T3® DCD® BNSS485IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- 3i T3® DCD® BNST610IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- 3i T3® DCD® BNST611IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- 3i T3® DCD® BNES365IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- 3i T3® DCD® BNES485IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- 3i T3® DCD® BNET3210IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- 3i T3® DCD® BNET3211IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- 3i T3® DCD® BNET3285IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- 3i T3® DCD® BNET410IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- 3i T3® DCD® BNET413IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- 3i T3® DCD® BNPS4313IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- 3i T3® DCD® BNSS310IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- 3i T3® DCD® BNST513IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- 3i T3® DCD® BNST685IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- 3i T3® DCD® BNPS6510IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- 3i T3® DCD® BNET3213IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- 3i T3® DCD® BNET511IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- 3i T3® DCD® BNET513IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- 3i T3® DCD® BNPS4311IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- 3i T3® DCD® BNPS5411IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- 3i T3® DCD® BNSS313IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- 3i T3® DCD® BNSS513IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- 3i T3® DCD® BNSS585IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- 3i T3® DCD® BNSS610IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- 3i T3® DCD® BNST515IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- 3i T3® DCD® BNST613IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- 3i T3® DCD® BNST615IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- 3i T3® DCD® BNPS5413IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- 3i T3® DCD® BNPS6513IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- 3i T3® DCD® BNPT6585IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- 3i T3® DCD® BNES410IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- 3i T3® DCD® BNES411IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- 3i T3® DCD® BNES415IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- 3i T3® DCD® BNES511IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- 3i T3® DCD® BNET611IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
Recent 3i T3 DCD adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 29, 2026Adverse Event Without Identified Device or Use Problem
The doctor reports that the dental implant failed due to peri-implantitis. Tooth site 45.The doctor reports in the PER that the procedure was not concluded by placing another implant.
Patient problems: Osteolysis; Unspecified Infection
MAUDE report 50931319 ↗InjurySep 14, 2026Adverse Event Without Identified Device or Use Problem
It was reported that the patient experienced pain since implant placement. The patient returned for a follow-up today and stated that the pain had decreased over the past 2 days, but the gums were sore to touch. The implant failed to integrate and an infection was observed. As a consequence, the implant was removed, the infection was cleaned, and a bone graft was placed. Tooth site 11. Patient suffered from pain.
Patient problems: Pain; Unspecified Infection
MAUDE report 50750984 ↗InjurySep 3, 2026Adverse Event Without Identified Device or Use Problem
The doctor reports that the dental implant failed due to peri-implantitis. Tooth site 36.The doctor reports in the PER that the procedure was not concluded by placing another implant.Inflammation and abscess were reported as a result of the event.
Patient problems: Abscess; Osteolysis; Unspecified Infection
MAUDE report 50582664 ↗InjuryJul 28, 2026Adverse Event Without Identified Device or Use Problem
It was reported that the implant at Tooth Site 12 was removed due to peri-implantitis. Inflammation was also reported.
Patient problems: Inflammation; Osteolysis; Unspecified Infection
MAUDE report 50055264 ↗InjuryJun 12, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT EXUDATE WAS NOTED AROUND THE IMPLANT AT TOOTH SITE #30 DURING CLEANING WITH PRESSURE AT THE SITE. A PA SHOWED A FAILING IMPLANT WITH MODERATE BONE LOSS. THE IMPLANT WAS REMOVED DUE TO BONE LOSS AND INFECTION.
Patient problems: Osteolysis; Unspecified Infection
MAUDE report 25490575 ↗InjuryJun 11, 2026Patient-Device Incompatibility
IT WAS REPORTED THAT IMPLANT WAS REMOVED DUE TO ALLERGIC REACTION. PATIENT REPORTED EDEMA AND DISCOMFORT ON X-RAY APPEARED TO BE ELICITING A REACTION AND BONE WAS RESORBING. TOOTH NUMBER 30. #30 IMPLANT REMOVED AND GRAFTED. SYMPTOMS AS A RESULT OF THE EVENT: PAIN, DISCOMFORT AND EDEMA.
Patient problems: Discomfort; Hypersensitivity/Allergic reaction; Pain
MAUDE report 25479129 ↗InjuryMay 13, 2026Adverse Event Without Identified Device or Use Problem
THE DOCTOR REPORTS THAT THE DENTAL IMPLANT LOCATED IN DENTAL POSITION NUMBER 34 FAILED DUE TO PERI-IMPLANTITIS. THE DOCTOR REPORTS THAT THE PROCEDURE WAS NOT CONCLUDED BY PLACING ANOTHER IMPLANT. THE DOCTOR REPORTED PAIN, INFLAMMATION AND ABSCESS.
Patient problems: Inflammation; Osteolysis; Unspecified Infection
MAUDE report 25159635 ↗InjuryMay 7, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #30 WAS REMOVED DUE TO PERI-IMPLANTITIS. IMPLANT HAS BONE LOSS AND INFECTION. SYMPTOMS AS A RESULT OF THE EVENT: PAIN.
Patient problems: Osteolysis; Pain; Unspecified Infection
MAUDE report 25117389 ↗InjuryApr 29, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #UNK WAS REMOVED DUE TO BONE LOSS. DENTIST FOUND MOBILITY OF IMPLANT. X-RAY SHOWS BONY SEQUESTRA FORMATION AT MESIAL ASPECT. REMOVED IMPLANT AND DISCOVERED FACIAL BONE WAS MISSING. BONE GRAFT SITE AND PATIENT TO RETURN FOR IMPLANT RE-PLACEMENT.
Patient problems: Osteolysis
MAUDE report 25034867 ↗InjuryApr 17, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #20 WAS REMOVED DUE TO PERI-IMPLANTITIS. THE IMPLANT WAS NOTED TO BE LOOSE AT THE ONE MONTH FOLLOW-UP EXAMINATION AND WAS REMOVED.
Patient problems: Osteolysis; Unspecified Infection
MAUDE report 24915514 ↗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 16, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #19 WAS REMOVED DUE TO PERI-IMPLANTITIS. PATIENT FAILED IST AND IMPLANT WAS REMOVED.
Patient problems: Osteolysis; Unspecified Infection
MAUDE report 24896609 ↗InjuryApr 10, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT DURING AN UNCOVER APPOINTMENT, THE IMPLANT AT TOOTH SITE #6 EXHIBITED PERI-IMPLANTITIS AND WAS REMOVED.
Patient problems: Osteolysis; Unspecified Infection
MAUDE report 24844954 ↗InjuryApr 10, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #10 WAS REMOVED DUE TO PERI-IMPLANTITIS. IMPLANT FAILED AND WAS REMOVED DURING UNCOVER.
Patient problems: Osteolysis; Unspecified Infection
MAUDE report 24840736 ↗MalfunctionApr 9, 2026Mechanical Problem
THE DOCTOR REPORTS THAT THE IMPLANT AT TOOTH SITE 36 HAS A DAMAGED HEXAGON AND WAS REMOVED. NO NEGATIVE IMPACT ON THE PATIENT¿S HEALTH WAS REPORTED AS A CONSEQUENCE OF THE EVENT. THE PROCEDURE WAS COMPLETED USING ANOTHER IMPLANT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24829765 ↗
Other ZimVie US Corp LLC products
- Tapered Screw-Vent131 models · 13,236 reports · 4 recalls
- OSSEOTITE CERTAIN74 models · 1,891 reports · 1 recall
- TSX Implants28 models · 1,279 reports
- OSSEOTITE73 models · 894 reports
- OSSEOTITE CERTAIN PREVAIL15 models · 785 reports
- CERTAIN BELLATEK12 models · 9 reports · 10 recalls
- Eztetic15 models · 382 reports
- Tapered SwissPlus12 models · 376 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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