Triathlon 5537-G-119Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327026986), received between Jun 17, 2021 and Jun 17, 2021 — classified as 1 injury.

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryJun 17, 2021Unstable; Unstable

  AS REPORTED: "REVISED THIS (RIGHT) KNEE FOR LIGAMENT INSTABILITY. WENT FROM A TS (1X19 INSERT TO A 1X25 INSERT). NO ALLEGATIONS AGAINST THE IMPLANTS. NO FURTHER INFORMATION WILL BE MADE AVAILABLE." REP PROVIDED PRIMARY AND REVISION USAGE REPORTS. SPOKE TO REP, WHO CONFIRMED THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.

  Patient problems: Joint Laxity

  MAUDE report 12014847 ↗