DJO SURGICAL 205-01-010Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888912109642), received between Oct 1, 2019 and Oct 1, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Loose or Intermittent Connection” (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.

• InjuryOct 1, 2019Loose or Intermittent Connection; Unstable

  REVISION SURGERY - THE PATIENT PRESENTED WITH PAIN AND INSTABILITY. PATIENT IS GROSSLY OVERWEIGHT AND SUFFERS FROM DIABETES AND OTHER HEALTH ISSUES. IT WAS DISCOVERED THAT BOTH THE TIBIA AND THE FEMUR HAD LOOSENED. ALL COMPONENTS WERE REMOVED. MORE AUGMENTS WERE USED AS WELL AS THE THICKER POLY.

  Patient problems: Failure of Implant; Pain

  MAUDE report 9139333 ↗