Triathlon 5510-F-102Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327040227), received between Sep 29, 2022 and Sep 29, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjurySep 29, 2022Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method

  THE INCORRECT FEMORAL COMPONENT WAS OPENED AND PLACED IN PATIENT. SURGERY WAS COMPLETED AND THE PATIENT WAS IN RECOVERY, WHEN REP REALIZED THE ISSUE. ONCE THE PATIENT WAS AWAKE, THEIR FAMILY AND THEM WERE NOTIFIED OF THE ISSUE AND PATIENT WAS BROUGHT BACK INTO THE OR. THE FEMORAL COMPONENT WAS SWAPPED SUCCESSFULLY. UPDATE: "THE INCORRECT IMPLANT PUT IN WAS A CEMENTED FEMUR WHEN IT WAS SUPPOSED TO BE A CEMENTLESS. SO, THE CEMENTED FEMORAL COMPONENT WAS PUT IN WITHOUT CEMENT."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15506788 ↗