Triathlon 5570-S-020Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327014990), received between Dec 7, 2017 and Jun 18, 2020 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Component Missing” (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 18, 2026.

Most reported problems

Recent adverse event reports

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

• InjuryJun 18, 2020Loss of Osseointegration; Loss of Osseointegration

  IT WAS REPORTED THAT THE PATIENT'S RIGHT KNEE WAS REVISED DUE TO LOOSENING. REVISING SURGEON REPORTED THAT CAUSE OR CONTRIBUTOR TO LOOSENING WAS DUE TO THE PRIOR SURGEON NOT USING ENOUGH CEMENT. THE PATIENT'S ENTIRE KNEE CONSTRUCT WAS REVISED. REP PROVIDED EXPLANT PICTURES AND REPORTED THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.

  Patient problems: Injury

  MAUDE report 10166541 ↗
• MalfunctionDec 7, 2017Component Missing; Component Missing

  DURING REVISION, THE NUT WAS MISSING IN THE OFFSET.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7096491 ↗