Triathlon 5532-P-711Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327042948), received between Aug 2, 2022 and Mar 21, 2023 — classified as 2 injuries.

The most frequently reported specific device problem is “Unstable” (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.

• InjuryMar 21, 2023Unstable; Unstable

  AS REPORTED: THE REVISION WAS SECONDARY TO INSTABILITY OF THE LEFT KNEE. THE USE OF MAKO WAS NOT THOUGHT TO BE THE CAUSE OF INSTABILITY." THE PATIENT'S NATIVE PATELLA WAS RESURFACED AND A 7X11 PS INSERT WAS REVISED TO A 7X16 TS INSERT.

  Patient problems: Joint Laxity

  MAUDE report 16583225 ↗
• InjuryAug 2, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AS REPORTED: "PLEASE FIND INFORMATION ON INDEX AND REVISION SURGERY PERFORMED ON A LEFT TOTAL KNEE REPLACEMENT. REVISION WAS DONE DUE TO INFECTION. NO FURTHER INFORMATION IS AVAILABLE FROM THE HOSPITAL OR DOCTOR."

  Patient problems: Unspecified Infection

  MAUDE report 15143497 ↗