Oxford Uni Knee System 32-422863Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05019279401895), received between Nov 18, 2019 and Nov 18, 2019 — classified as 1 malfunction.

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

• MalfunctionNov 18, 2019Fitting Problem; Fitting Problem

  IT WAS REPORTED BY THE HOSPITAL THAT DURING STERILIZATION THE INSTRUMENT WAS DISASSEMBLED FOR CLEANING. SUBSEQUENTLY, THE INSTRUMENT WOULD NOT FUNCTION CORRECTLY. THE CONNECTION OF THE OXF TIB RESECT STYLUS ASSY (BOTH VERSIONS) TO THE OXFORD TIBIAL GAP GAUGE WAS NOT WORKING PROPERLY.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9334587 ↗