Oxford Partial Knee System 159569Recalls & reported problems

Summary

The FDA's MAUDE database contains 16 adverse event reports that list this exact device (DI 05019279786152), received between Jun 5, 2019 and Jan 2, 2026 — classified as 14 injuries, 2 malfunctions.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (5 reports).

22 other recalls cover devices cleared under the same FDA submission (P010014); they may or may not involve this specific model.

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 16 most recent of 16 reports, in the reporter's own words as published by the FDA.

• InjuryJan 2, 2026Adverse Event Without Identified Device or Use Problem

  NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Insufficient Information

  MAUDE report 23941891 ↗
• InjuryNov 26, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated

  NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Joint Dislocation; Pain

  MAUDE report 23655120 ↗
• MalfunctionSep 9, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Pain

  MAUDE report 20168461 ↗
• InjuryDec 18, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT: A PATIENT HAD A KNEE ARTHROPLASTY AND SUBSEQUENTLY A REVISION SURGERY WAS PERFORMED DUE TO THE DISLOCATION OF THE BEARING. DUE DILIGENCE IS IN PROGRESS FOR THIS COMPLAINT; TO DATE NO ADDITIONAL INFORMATION OR PRODUCT HAS BEEN RECEIVED.

  Patient problems: Joint Dislocation

  MAUDE report 18343141 ↗
• InjuryOct 5, 2023Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth

  NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Ambulation or Postural Difficulties; Cramp(s) /Muscle Spasm(s); Failure of Implant; Pain; Swelling/ Edema

  MAUDE report 17874620 ↗
• InjuryAug 31, 2023Patient Device Interaction Problem; Patient Device Interaction Problem

  IT WAS REPORTED THAT PATIENT UNDERWENT A PARTIAL KNEE ARTHROPLASTY AND APPROXIMATELY 5 YEARS LATER A REVISION SURGERY WAS PERFORMED DUE TO WEAR AND KNEE PAIN. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Pain

  MAUDE report 17660595 ↗
• InjuryAug 17, 2023Patient Device Interaction Problem; Patient Device Interaction Problem

  IT WAS REPORTED THAT PATIENT UNDERWENT KNEE PROSTHESES IMPLANTATION APPROXIMATELY SIX (6) YEARS AGO. ABOUT SIX (6) YEARS LATER PATIENT COMPLAINED OF KNEE PAIN, RESULTING IN REVISION SURGERY WITH EXCHANGING KNEE PROSTHESES. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Pain

  MAUDE report 17562680 ↗
• InjurySep 8, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT PATIENT UNDERWENT REVISION OF KNEE PROSTHESIS DUE TO BEARING DISLOCATION IN UNKNOWN TIME FRAME POST-OP. DUE DILIGENCE IS IN PROGRESS FOR THIS COMPLAINT; TO DATE NO ADDITIONAL INFORMATION OR PRODUCT HAS BEEN RECEIVED.

  Patient problems: Joint Dislocation

  MAUDE report 15376344 ↗
• InjurySep 5, 2022Unintended Movement; Unintended Movement

  IT WAS REPORTED THAT THE PATIENT HAD AN INITIAL RIGHT KNEE ARTHROPLASTY AND APPROXIMATELY 1.5 YEARS LATER A REVISION SURGERY WAS PERFORMED DUE TO THE LUXATION OF THE INLAY. IT WAS ALSO REPORTED THAT THE SURFACE OF THE EXPLANTED PRODUCT WAS NOT AS SMOOTH AS EXPECTED. DUE DILIGENCE IS IN PROGRESS FOR THIS COMPLAINT; TO DATE NO ADDITIONAL INFORMATION OR PRODUCT HAS BEEN RECEIVED.

  Patient problems: Joint Dislocation

  MAUDE report 15354614 ↗
• InjuryJun 24, 2022Unstable; Unstable

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION SURGERY DUE TO INSTABILITY APPROXIMATELY 4 YEARS AFTER IMPLANTATION. THE PATIENT HAS BEEN REVISED FROM A 4MM BEARING TO A 6MM BEARING. NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME.

  Patient problems: Failure of Implant

  MAUDE report 14796632 ↗
• InjuryJan 14, 2022Patient Device Interaction Problem; Patient Device Interaction Problem

  IT WAS REPORTED, THAT: IT WAS REPORTED THAT A PATIENT UNDERWENT AN INITIAL RIGHT KNEE ARTHROPLASTY ON AN UNKNOWN DATE. SUBSEQUENTLY, THE SMALL RIGHT 4MM BEARING WAS REMOVED ON (B)(6) 2022 AS THE METAL X-RAY MARKER CAME OUT OF THE BEARING AND WAS IRRITATING THE PATIENT'S SOFT TISSUES. BEARING WAS REMOVED AND REPLACE WITH A NEW BEARING OF THE SAME SIZE. PATIENT INVOLVEMENT - REVISION.

  Patient problems: Implant Pain

  MAUDE report 13257698 ↗
• InjuryMay 27, 2021Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT A PATIENT UNDERWENT AN INITIAL RIGHT KNEE ARTHROPLASTY ON AN (B)(6) 2017 SUBSEQUENTLY, A REVISION PROCEDURE DUE TO BEARING DISLOCATION WAS PERFORMED ON (B)(6) 2021.

  Patient problems: Joint Dislocation

  MAUDE report 11892887 ↗
• InjuryDec 17, 2020Mechanical Problem; Device Dislodged or Dislocated; Unintended Movement; Mechanical Problem; Device Dislodged or Dislocated; Unintended Movement

  IT WAS REPORTED THAT A PATIENT UNDERWENT AN INITIAL RIGHT KNEE ARTHROPLASTY ON (B)(6) 2020. SUBSEQUENTLY, A REVISION PROCEDURE DUE TO DISLOCATION WAS PERFORMED ON (B)(6) 2020 WHEN THE BEARING WAS REVISED TO A DIFFERENT THICKNESS.

  Patient problems: Joint Dislocation

  MAUDE report 11026588 ↗
• MalfunctionOct 2, 2020Delivered as Unsterile Product; Device Damaged Prior to Receipt by User; Manufacturing, Packaging or Shipping Problem; Delivered as Unsterile Product; Device Damaged Prior to Receipt by User; Manufacturing, Packaging or Shipping Problem

  BEFORE OPENING THE LAST LAYER OF ASEPTIC PACKAGING (STILL SEALED), IT WAS FOUND THAT THERE WAS A HAIR ON THE OXFORD PHASE 3 ANATOMIC ARCOM BEARING. THE DOCTOR USED THE SAME TYPE OF PRODUCT WITH DIFFERENT THICKNESS OF 3MM TO COMPLETE THE OPERATION. THE OPERATION WAS DELAYED FOR 10 MINUTES.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10619461 ↗
• InjuryApr 7, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED BY CRF REPORT FOR STUDY OXFORD_U3030 THAT THE PATIENT EXPERIENCED TINGLING AND IN EDEMA ON RIGHT KNEE. NO TRAUMA REPORTED.

  Patient problems: Joint Swelling

  MAUDE report 9932165 ↗
• InjuryJun 5, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  IT WAS REPORTED THAT A PATIENT UNDERWENT A RIGHT KNEE REPLACEMENT PROCEDURE. SUBSEQUENTLY, THE PATIENT UNDERWENT SURGERY DUE TO WOUND COMPLICATIONS.

  Patient problems: Wound Dehiscence

  MAUDE report 8669510 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under P010014. One submission often covers many models, so check the product and lot details in each record.

• Z-1164-2017 · Jan 5, 2016 · Terminated
  Oxford Partial Knee System Right Medial Tibial Trial Tray Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System
• Z-1152-2017 · Jan 5, 2016 · Terminated
  Oxford Knee System Tibial Resector Body Tube & Guides Product Usage: Instruments for use with the Oxford Uni Partial Knee System
• Z-1162-2017 · Jan 5, 2016 · Terminated
  Oxford Partial Knee System Right Medial Tibial Trial Tray Size D Product Usage: Instruments for use with the Oxford Uni Partial Knee System
• Z-1171-2017 · Jan 5, 2016 · Terminated
  Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size D Product Usage: Instruments for use with the Oxford Uni Partial Knee System
• Z-1172-2017 · Jan 5, 2016 · Terminated
  Oxford Partial Knee System Phase 3 Tibial Template Left Medial Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System
• Z-1160-2017 · Jan 5, 2016 · Terminated
  Oxford Partial Knee System Right Medial Tibial Trial Tray Size E Product Usage: Instruments for use with the Oxford Uni Partial Knee System
• Z-1159-2017 · Jan 5, 2016 · Terminated
  Oxford Partial Knee System Left Medial Tibial Trial Tray Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System
• Z-1173-2017 · Jan 5, 2016 · Terminated
  Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System
• Z-1170-2017 · Jan 5, 2016 · Terminated
  Oxford Unicompartmental Knee Phase 3 Shim Size 1 Product Usage: Instruments for use with the Oxford Uni Partial Knee System
• Z-1155-2017 · Jan 5, 2016 · Terminated
  Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System
• Z-1153-2017 · Jan 5, 2016 · Terminated
  Oxford Partial Knee System Femoral Slap Hammer Product Usage: Instruments for use with the Oxford Uni Partial Knee System
• Z-1154-2017 · Jan 5, 2016 · Terminated
  Oxford Unicompartmental Knee Phase 3 Tibial Impactor Product Usage: Instruments for use with the Oxford Uni Partial Knee System
• Z-1165-2017 · Jan 5, 2016 · Terminated
  Oxford Partial Knee System Right Medial Tibial Trial Tray Size C Oxford Partial Knee System Left Medial Tibial Trial Tray Size C
• Z-1169-2017 · Jan 5, 2016 · Terminated
  Oxford Unicompartmental Knee Phase 3 Shim Size 2 Product Usage: Instruments for use with the Oxford Uni Partial Knee System
• Z-1156-2017 · Jan 5, 2016 · Terminated
  Oxford Partial Knee System Right Medial Tibial Trial Tray Size F Product Usage: Instruments for use with the Oxford Uni Partial Knee System

…and 7 more.