3i T3 SHORTRecalls & reported problems across all models
ZimVie US Corp LLC · 4 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 97
- Deaths reported
- 0
- Injuries reported
- 90
- Recalls
- 0
We found 4 models of 3i T3 SHORT by ZimVie US Corp LLC in the FDA's device registry (GUDID). Together they are named in 97 adverse event reports in the FDA's MAUDE database, received between May 23, 2019 and May 7, 2026 — classified as 90 injuries, 7 malfunctions.
The most frequently reported specific device problem is “Separation Failure” (9 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 SHORT problems
Device problems
- Adverse Event Without Identified Device or Use Problem83
- Separation Failure9
- Mechanical Problem4
- Component Missing1
- Failure to Disconnect1
- Fracture1
- Loss of Osseointegration1
Patient problems
- Osteolysis43
- Unspecified Infection41
- No Clinical Signs, Symptoms or Conditions21
- Pain21
- Inflammation20
- No Information7
- No Code Available6
- Swelling/ Edema4
3i T3 SHORT models
4 models, most reported first. Each model has its own page with its reports, recalls and device details.
- 3i T3® SHORT BOES505IMPLANT, ENDOSSEOUS, ROOT-FORM34 reports
- 3i T3® SHORT BOES506IMPLANT, ENDOSSEOUS, ROOT-FORM26 reports
- 3i T3® SHORT BOES605IMPLANT, ENDOSSEOUS, ROOT-FORM21 reports
- 3i T3® SHORT BOES606IMPLANT, ENDOSSEOUS, ROOT-FORM16 reports
Recent 3i T3 SHORT adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryMay 7, 2026Adverse Event Without Identified Device or Use Problem
THE DOCTOR REPORTS THAT THE DENTAL IMPLANT LOCATED IN DENTAL POSITION NUMBER #26 FAILED DUE TO PERI-IMPLANTITIS. THE DOCTOR REPORTS IN THE FORM THAT THE PROCEDURE WAS CONCLUDED BY PLACING ANOTHER IMPLANT.
Patient problems: Osteolysis; Unspecified Infection
MAUDE report 25110190 ↗InjuryApr 1, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT IMPLANT IN SITE 15 WAS REMOVED. IMPLANT FAILED DUE TO INFECTION.
Patient problems: Unspecified Infection
MAUDE report 24752792 ↗InjuryMar 30, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THE IMPLANT WAS REMOVED FROM TOOTH SITE #26 DUE TO BONE LOSS. NO OTHER IMPACT ON THE PATIENT REPORTED.
Patient problems: Osteolysis
MAUDE report 24725468 ↗InjuryMar 30, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT IMPLANT AT TOOTH SITE 26 WAS REMOVED DUE TO BONE LOSS. NO OTHER IMPLANT WAS PLACED DURING THE SAME PROCEDURE.
Patient problems: Osteolysis
MAUDE report 24725180 ↗InjuryFeb 17, 2026Mechanical Problem
NO ADDITIONAL EVENT INFORMATION RECEIVED AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24369889 ↗MalfunctionFeb 4, 2026Component Missing
DOCTOR REPORTS THAT WHEN THEY OPENED THE PACKAGING THERE WAS NO IMPLANT INSIDE. THE PROCEDURE WAS COMPLETED USING ANOTHER IMPLANT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24256306 ↗InjuryJan 8, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE # 17 WAS REMOVED DUE TO PERI-IMPLANTITIS. SYMPTOMS AS A RESULT OF THE EVENT: PAIN.
Patient problems: Osteolysis; Pain; Unspecified Infection
MAUDE report 24013417 ↗InjuryDec 9, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #3 WAS REMOVED DUE TO PERI-IMPLANTITIS. SYMPTOMS AS A RESULT OF THE EVENT: INFLAMMATION.
Patient problems: Inflammation; Osteolysis; Unspecified Infection
MAUDE report 23758137 ↗InjuryDec 8, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #46 WAS REMOVED DUE TO BONE LOSS.
Patient problems: Osteolysis
MAUDE report 23736612 ↗InjuryJul 30, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
NO ADDITIONAL EVENT INFORMATION RECEIVED AT THE TIME OF THIS REPORT.
Patient problems: Unspecified Infection
MAUDE report 22672413 ↗InjuryJul 28, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT IMPLANT WAS REMOVED DUE TO BONE LOSS. PATIENT COMPLAINED OF PAIN AND FELT THE IMPLANT TOOTH WAS LOOSE, CLINICALLY, IMPLANT WAS MOBILE AND X-RAY REVEALED SEVERE CIRCUMFERENTIAL BONE LOSS, IMPLANT WAS REMOVED ON THE DAY. TOOTH SITE # 47. SYMPTOMS AS A RESULT OF THE EVENT: INFLAMMATION, PAIN.
Patient problems: Inflammation; Osteolysis; Pain
MAUDE report 22628947 ↗InjuryJul 15, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT IMPLANT AT TOOTH SITE #3 WAS REMOVED DUE TO BONE LOSS AND INFECTION. STAGE TWO PLACEMENT OF HEALING ABUTMENT ATTEMPTED BUT MODERATE BONE LOSS AROUND IMPLANT AND INCREASED SENSITIVITY, IMPLICATING INFECTION. SYMPTOMS AS A RESULT OF THE EVENT: PAIN AND INFLAMMATION.
Patient problems: Osteolysis; Pain; Unspecified Infection
MAUDE report 22505782 ↗InjuryJun 9, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED A PERI-IMPLANTITIS AT TOOTH SITE 47 OBSERVED DURING EXAMINATION AND X-RAYS. THE PATIENT WENT TO THE CLINIC DUE TO INFLAMMATION AND BONE LOSS WAS ALSO DETECTED. IMPLANT WAS REMOVED. THE PROCESS WAS COMPLETED WITH ANOTHER IMPLANT.
Patient problems: Inflammation; Osteolysis; Unspecified Infection
MAUDE report 22165429 ↗InjuryJun 9, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
SCREW-RETAINED IMPLANT-SUPPORTED BRIDGE ON IMPLANTS AT TOOTH POSITIONS 15 AND 16. IT WAS REPORTED A PERI-IMPLANTITIS AT TOOTH SITE 16. IT WAS DETECTED AND UNSUCCESSFUL TREATED IN 2024. FINALLY IMPLANT WAS REMOVED ON (B)(6) 2025 DUE TO PERIIMPLANTITIS (B)(4). THE PROCESS WAS NOT COMPLETED WITH ANOTHER IMPLANT. IMPACT REPORTED ON THE PATIENT: INFLAMMATION THIS EVENT REFERS TO 2024 PERI-IMPLANTITIS TREATMENT.
Patient problems: Inflammation; Osteolysis; Unspecified Infection
MAUDE report 22164993 ↗InjuryJun 9, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
SCREW-RETAINED IMPLANT-SUPPORTED BRIDGE ON IMPLANTS AT TOOTH POSITIONS 15 AND 16. IT WAS REPORTED A PERI-IMPLANTITIS AT TOOTH SITE 16. IT WAS DETECTED AND UNSUCCESSFUL TREATED IN 2024 (B)(4). IMPLANT WAS REMOVED. THE PROCESS WAS NOT COMPLETED WITH ANOTHER IMPLANT. IMPACT REPORTED ON THE PATIENT: INFLAMMATION
Patient problems: Inflammation; Osteolysis; Unspecified Infection
MAUDE report 22164978 ↗
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
- 3i T3 DCD73 models · 789 reports
- OSSEOTITE CERTAIN PREVAIL15 models · 785 reports
- CERTAIN BELLATEK12 models · 9 reports · 10 recalls
- Eztetic15 models · 382 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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