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
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 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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