ADVANCE® KPON32MBRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI M684KPON32MB1), received between Aug 18, 2020 and Apr 3, 2024 — classified as 2 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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.

• InjuryApr 3, 2024Loss of Osseointegration; Noise, Audible; Loss of Osseointegration; Noise, Audible

  ALLEGEDLY, WHILE PATIENT CLIMBING INTO BED THE KNEE POPPED OUT AND HAD PAIN. DOCTOR SAYS THAT THE KNEE CAP PIECE HAD DETACHED AND WAS FLOATING AROUND THE LEG. A REVISION SURGERY WAS PERFORMED TO REMOVE THE DETACHED PATELLA AND REPLACE IT WITH ONE THAT CEMENTS IT.

  Patient problems: Pain

  MAUDE report 19034278 ↗
• InjuryAug 18, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

  ALLEGEDLY, PATIENT WAS REVISED DUE TO FEMORAL COMPONENT OVERSIZED, AND THE PATIENT MOTION WAS QUITE LIMITED, WITH A RANGE OF 0 TO 30 DEGREES, WITH A HARD STOP AT 30 DEGREES.

  Patient problems: Loss of Range of Motion

  MAUDE report 10420884 ↗