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OSSEOTITE® FNT415Recalls & reported problems

ZimVie US Corp LLC · FULL OSSEOTITE® TAPERED IMPLANT 4 X 15MM · Class 2 · Implant

All models of OSSEOTITE (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 00844868003359), received between Dec 10, 2019 and Mar 3, 2020 — classified as 2 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 16, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem2

Patient problems

  • Unspecified Infection2
  • Pain1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryMar 3, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    DOCTOR REPORTS THAT THE FNT415 IMPLANT WAS REMOVED DUE TO INFECTION. PAIN IS ALSO REPORTED. TOOTH SITE #6.

    Patient problems: Pain; Unspecified Infection

    MAUDE report 9782588 ↗
  • InjuryDec 10, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE WAS IMPLANT REMOVED DUE TO INFECTION.

    Patient problems: Unspecified Infection

    MAUDE report 9443176 ↗

Other IMPLANT, ENDOSSEOUS, ROOT-FORM devices

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Sources and updates

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