3i T3® DCD® BNET3213Recalls & reported problems
ZimVie US Corp LLC · 3I T3® WITH DCD® EX HEX TAPERED IMPLANT 3.25 X 13MM · Class 2 · Implant
All models of 3i T3 DCD (73)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00844868033028), received between Jun 19, 2020 and Feb 15, 2023 — classified as 2 injuries.
The most frequently reported specific device problem is “Fracture” (1 report).
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 16, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Fracture1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- Unspecified Infection1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryFeb 15, 2023Fracture; Fracture
IT WAS REPORTED THAT THE DENTAL IMPLANT LOCATED IN AN UNKNOWN POSITION FAILED BECAUSE IT FRACTURED ON THE HEXAGON PART, THE DOCTOR INDICATES IN THE PER THAT THE PROCEDURE WAS NOT CONCLUDED WITH THE PLACEMENT OF ANOTHER IMPLANT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16383575 ↗InjuryJun 19, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE DOCTOR REPORTED THAT THE IMPLANT BNET3213 WAS REMOVED DUE TO INFECTION AND PAIN. THE DOCTOR PLACED A NEW IMPLANT IN THE SAME INTERVENTION.
Patient problems: Unspecified Infection
MAUDE report 10173220 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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