3i T3® BOST410Recalls & reported problems
ZimVie US Corp LLC · 3i T3® NON-PLATFORM SWITCHED TAPERED IMPLANT 4 X 10MM · Class 2 · Implant
Quick summary
This ZimVie 3i T3 dental implant has 210 adverse event reports, with no deaths and 206 injuries. Most describe infection around the implant, often with bone loss, and some say the implant had to be removed. Pain is also commonly mentioned. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 211
- Deaths reported
- 0
- Injuries reported
- 207
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 211 adverse event reports that list this exact device (DI 00844868028925), received between Sep 26, 2019 and Jul 27, 2026 — classified as 207 injuries, 4 malfunctions.
The most frequently reported specific device problem is “Fracture” (12 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, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem191
- Fracture12
- Mechanical Problem6
- Patient-Device Incompatibility1
- Positioning Failure1
Patient problems
- Unspecified Infection135
- Osteolysis102
- Pain54
- Inflammation34
- No Clinical Signs, Symptoms or Conditions32
- No Code Available15
- Abscess11
- Swelling/ Edema11
Recent adverse event reports
The 25 most recent of 211 reports, in the reporter's own words as published by the FDA.
InjuryJul 27, 2026Adverse Event Without Identified Device or Use Problem
It was reported that two implants at tooth sites 15 and 11 were removed due to a loss of integration and a severe peri-implantitis. Subsequent sanitation with photographs will be performed 1 and 2 months after the loss of the implants.
Patient problems: Osteolysis; Unspecified Infection
MAUDE report 50017254 ↗InjuryMay 12, 2026Adverse Event Without Identified Device or Use Problem
DOCTOR REPORTED THAT IMPLANT AT TOOTH SITE 35 WAS REMOVED DUE TO PERI-IMPLANTITIS WITH INFLAMMATION, PAIN AND SWELLING. PATIENT HAS BEEN RESCHEDULED FOR NEW IMPLANTATION LATER ON.
Patient problems: Osteolysis; Swelling/ Edema; Unspecified Infection
MAUDE report 25146964 ↗InjuryApr 23, 2026Adverse Event Without Identified Device or Use Problem
THE DOCTOR REPORTS THAT THE DENTAL IMPLANTS LOCATED IN DENTAL POSITIONS 25 AND 27 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 24964103 ↗InjuryMar 30, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT DEVELOPED AN INFECTION AND HAS LOST BONE HEIGHT THAT COULD COMPROMISE INTEGRATION, SO IMPLANT AT TOOTH SITE 37 WAS REMOVED . PAIN WAS REPORTED AS A CONSEQUENCE OF THE EVENT.
Patient problems: Osteolysis; Pain; Unspecified Infection
MAUDE report 24725728 ↗InjuryFeb 24, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANTS AT TOOTH SITES #35 AND #44 WERE REMOVED DUE TO PERI-IMPLANTITIS.
Patient problems: Osteolysis; Unspecified Infection
MAUDE report 24434684 ↗InjuryFeb 13, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #22 WAS REMOVED DUE TO PERI-IMPLANTITIS.
Patient problems: Osteolysis; Unspecified Infection
MAUDE report 24339819 ↗InjuryFeb 11, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT IMPLANT WAS REMOVED DUE TO PERI-IMPLANTITIS. SPONTANEOUS EXFOLIATION OF IMPLANT. PATIENT REPORTED THE LOSS OF THE IMPLANT SHORTLY AFTER CHRISTMAS, STATED THAT THE IMPLANT "FELL OUT.". SYMPTOMS AS A RESULT OF THE EVENT: PAIN.
Patient problems: Osteolysis; Pain; Unspecified Infection
MAUDE report 24317209 ↗InjuryFeb 10, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT DURING AN EXAM, BONE LOSS WAS NOTED AROUND THE IMPLANT AT TOOTH SITE #20. THE IMPLANT WAS REMOVED. SYMPTOMS AS A RESULT OF THE EVENT: PAIN.
Patient problems: Osteolysis; Pain
MAUDE report 24305581 ↗InjuryFeb 4, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT IMPLANT #11 FAILED, BUCCAL BONE FRACTURED.
Patient problems: Bone Fracture(s)
MAUDE report 24257084 ↗InjuryJan 13, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #35 WAS REMOVED DUE TO PERI-IMPLANTITIS. SYMPTOMS AS A RESULT OF THE EVENT: INFLAMMATION.
Patient problems: Inflammation; Osteolysis; Unspecified Infection
MAUDE report 24058286 ↗InjuryJan 13, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #46 WAS REMOVED DUE TO PERI-IMPLANTITIS. SYMPTOMS AS A RESULT OF THE EVENT: INFLAMMATION.
Patient problems: Inflammation; Osteolysis; Unspecified Infection
MAUDE report 24058168 ↗InjuryJan 8, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANTS WERE REMOVED DUE TO INFECTION. SYMPTOMS AS A RESULT OF THE EVENT: INFLAMMATION.
Patient problems: Inflammation; Unspecified Infection
MAUDE report 24008159 ↗InjuryJan 7, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT IMPLANT FAILED DUE TO INFECTION IN THE BONE. TOOTH NUMBER 6.
Patient problems: Unspecified Infection
MAUDE report 23989789 ↗InjuryDec 22, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT IMPLANT WITH CRESTAL FISTULAS OVER COVER SCREW. EXPLORED AND IMPLANT LOOSE WITH BONE RESORPTION.
Patient problems: Fistula
MAUDE report 23863499 ↗InjuryDec 8, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANTS AT TOOTH SITES #35 AND #36 WERE REMOVED DUE TO INFECTION.
Patient problems: Unspecified Infection
MAUDE report 23736172 ↗InjuryNov 22, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT AN IMPLANT AT TOOTH SITE # 46 WAS REMOVED DUE TO A PERI-IMPLANTITIS. PATIENT SUFFERED FROM PAIN AND INFLAMMATION.
Patient problems: Inflammation; Osteolysis; Unspecified Infection
MAUDE report 23625153 ↗InjuryNov 10, 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: Inflammation; Swelling/ Edema; Unspecified Infection
MAUDE report 23510566 ↗InjuryOct 28, 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 #13 WAS REMOVED DUE TO BONE LOSS AROUND THE IMPLANT AT THE TIME OF 2ND STAGE. NO INFLAMMATION OR SWELLING OF SURROUNDING MUCOSAL TISSUE.
Patient problems: Osteolysis
MAUDE report 23403657 ↗InjurySep 8, 2025Fracture; Fracture
IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #16 FRACTURED WAS REMOVED. SYMPTOMS AS A RESULT OF THE EVENT: PAIN & EDEMA.
Patient problems: Pain; Swelling/ Edema
MAUDE report 22991962 ↗InjurySep 3, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE DENTAL IMPLANT LOCATED IN POSITION # 32 FAILED DUE TO PERI-IMPLANTITIS.
Patient problems: Osteolysis; Unspecified Infection
MAUDE report 22951227 ↗InjuryAug 18, 2025Adverse 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 #47. PATIENT SUFFERED PAIN AND INFLAMMATION.
Patient problems: Osteolysis; Pain; Unspecified Infection
MAUDE report 22833880 ↗InjuryJul 28, 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 #35 WAS REMOVED DUE TO PERI-IMPLANTITIS. SYMPTOMS AS A RESULT OF THE EVENT: INFLAMMATION.
Patient problems: Inflammation; Osteolysis; Unspecified Infection
MAUDE report 22634547 ↗InjuryJun 16, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED PERIIMPLANTITIS AT TOOTH SITE #46. PAIN WAS REPORTED AS A RESULT OF THE EVENT. IMPLANT WAS REMOVED.
Patient problems: Osteolysis; Pain; Unspecified Infection
MAUDE report 22209690 ↗InjuryJun 9, 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 22167942 ↗InjuryMay 27, 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 #16 WAS REMOVED DUE TO PERI-IMPLANTITIS. SYMPTOMS AS A RESULT OF THE EVENT: INFLAMMATION.
Patient problems: Inflammation; Osteolysis; Unspecified Infection
MAUDE report 22090563 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.