3i T3® DCD® BNPT5415Recalls & reported problems
ZimVie US Corp LLC · 3i T3® WITH DCD® TAPERED IMPLANT 5/4 X 15MM · Class 2 · Implant
All models of 3i T3 DCD (73)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00844868029496), received between Nov 6, 2020 and Sep 12, 2023 — classified as 4 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.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem4
Patient problems
- Unspecified Infection3
- Osteolysis2
- Inflammation1
- Pain1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjurySep 12, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT PATIENT PRESENTED WITH PAIN (UNBEARABLE) REQUESTED TO HAVE IMPLANT REMOVED. TOOTH #4. SYMPTOMS AS A RESULT OF THE EVENT: PAIN.
Patient problems: Pain
MAUDE report 17732988 ↗InjuryOct 22, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE # 29 LOST INTEGRATION DUE TO PERI-IMPLANTITIS AT THE IMPLANT SITE AND WAS REMOVED. DURING THE IMPLANT STABILITY TEST THERE WAS PURULENT DRAINAGE FROM THE IMPLANT SITE 29. THE IMPLANT WAS INCOMPLETE INTEGRATION OF THE IMPLANT AT THIS SITE.
Patient problems: Osteolysis; Unspecified Infection
MAUDE report 12682258 ↗InjuryJul 22, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #9 WAS REMOVED DUE TO PERIIMPLANTITIS. INFLAMMATION AND SINUS DRAINAGE ON FACIAL REPORTED AS SYMPTOMS.
Patient problems: Inflammation; Osteolysis; Unspecified Infection
MAUDE report 12213077 ↗InjuryNov 6, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IMPLANT WAS REMOVED DUE TO INFECTION. TOOTH LOCATION 33.
Patient problems: Unspecified Infection
MAUDE report 10805206 ↗
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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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