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3i T3® BOST3215Recalls & reported problems

ZimVie US Corp LLC · 3i T3® NON-PLATFORM SWITCHED TAPERED IMPLANT 3.25 X 15MM · Class 2 · Implant

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
16
Deaths reported
0
Injuries reported
16
Recalls naming it
0

Summary

The FDA's MAUDE database contains 16 adverse event reports that list this exact device (DI 00844868028901), received between Jan 14, 2021 and Apr 3, 2026 — classified as 16 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 18, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 3 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 1 reportsJul 2024: 0 reportsAug 2024: 1 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 1 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 1 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520263
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem16

Patient problems

  • Unspecified Infection13
  • Osteolysis10
  • Pain5
  • Inflammation3
  • No Clinical Signs, Symptoms or Conditions2
  • Hypersensitivity/Allergic reaction1
  • No Code Available1
  • Swelling/ Edema1

Recent adverse event reports

The 16 most recent of 16 reports, in the reporter's own words as published by the FDA.

  • InjuryApr 3, 2026Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #7 WAS REMOVED DUE TO LOSS OF INTEGRATION ASSOCIATED WITH PERI-IMPLANTITIS. IT WAS NOTED TO HAVE COME LOOSE WITH THE PATIENT BIT THE IMPLANT.

    Patient problems: Osteolysis; Unspecified Infection

    MAUDE report 24781515 ↗
  • InjuryJan 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 #11 WAS REMOVED DUE TO PERI-IMPLANTITIS.

    Patient problems: Osteolysis; Unspecified Infection

    MAUDE report 21252154 ↗
  • InjuryAug 20, 2024Adverse 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: Osteolysis; Pain

    MAUDE report 20008639 ↗
  • InjuryJun 20, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #28 WAS MOBILE AND TENDER AND WAS REMOVED DUE TO INFECTION. SYMPTOMS AS A RESULT OF THE EVENT: PAIN & EDEMA.

    Patient problems: Pain; Swelling/ Edema; Unspecified Infection

    MAUDE report 19576027 ↗
  • InjuryMar 28, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED A PERIIMPLANTITIS AT TOOTH SITE 24. PATIENT SUFFERED INFLAMMATION. IMPLANT WAS REMOVED.

    Patient problems: Inflammation; Osteolysis; Unspecified Infection

    MAUDE report 18993300 ↗
  • InjuryMar 18, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE IMPLANT IN TOOTH SITE # 26 WAS REMOVED WHEN PT RETURNED TO OFFICE FOR STABILITY CHECK AND PERI-IMPLANTITIS WAS NOTED. SYMPTOMS AS A RESULT OF THE EVENT: PAIN.

    Patient problems: Osteolysis; Pain; Unspecified Infection

    MAUDE report 18924934 ↗
  • InjuryMar 15, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE IMPLANT IN TOOTH SITE # 24 WAS REMOVED WHEN PT RETURNED TO OFFICE FOR STABILITY CHECK AND PERI-IMPLANTITIS WAS NOTED. SYMPTOMS AS A RESULT OF THE EVENT: PAIN.

    Patient problems: Osteolysis; Pain; Unspecified Infection

    MAUDE report 18918513 ↗
  • InjuryAug 22, 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 #25 WAS REMOVED DUE TO PERI-IMPLANTITIS. SYMPTOMS AS A RESULT OF THE EVENT: INFLAMMATION.

    Patient problems: Inflammation; Osteolysis; Unspecified Infection

    MAUDE report 17594883 ↗
  • InjuryAug 4, 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 #10 WAS INFECTED AT UNCOVERING. THE IMPLANT WITH CROWN ATTACHED WAS REMOVED DUE TO PERI-IMPLANTITIS.

    Patient problems: Osteolysis; Unspecified Infection

    MAUDE report 17459109 ↗
  • InjuryJun 29, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

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

    Patient problems: Osteolysis; Unspecified Infection

    MAUDE report 17231468 ↗
  • InjuryMay 6, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    CUSTOMER REPORTED INFECTION/PAIN AT TOOTH SITE #23. THE IMPLANT WAS REMOVED. SYMPTOMS AS A RESULT OF THE EVENT: INCREASED FISTULAS. FLAP-IMPLANT MOBILE.

    Patient problems: Pain; Unspecified Infection

    MAUDE report 14306875 ↗
  • InjuryJan 14, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED BY CUSTOMER THAT THE IMPLANT WAS REMOVED DUE TO INFECTION AND ALLERGIC REACTION.

    Patient problems: Hypersensitivity/Allergic reaction; Unspecified Infection

    MAUDE report 13261328 ↗
  • InjuryMay 15, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED IMPLANT AT TOOTH LOCATION # 9 WAS REMOVED DUE TO LACK OF PRIMARY STABILITY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11829952 ↗
  • InjuryMar 19, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    DOCTOR REPORTED PERI-IMPLANTITIS WITH DEHISCENSE AT TOOTH SITE 22 (FDI).

    Patient problems: Osteolysis; Unspecified Infection; Wound Dehiscence

    MAUDE report 11527528 ↗
  • InjuryMar 17, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE IMPLANT WAS UNABLE TO BE PLACED DUE TO A LACK OF PRIMARY STABILITY. SITE WAS GRAFTED AND PATIENT WILL RETURN FOR A NEW IMPLANT. TOOTH #10.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11507101 ↗
  • InjuryJan 14, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE BOST3215 IMPLANT AT TOOTH SITE #23 WAS REMOVED DUE TO INFECTION AND BONE LOSS. SITE GRAFTED. INFLAMMATION IS ALSO REPORTED.

    Patient problems: Inflammation; No Code Available; Unspecified Infection

    MAUDE report 11169847 ↗

Other IMPLANT, ENDOSSEOUS, ROOT-FORM devices

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Sources and updates

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