Oxford Partial Knee System 159541Recalls & reported problems

Summary

The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI 05019279785872), received between Jun 21, 2019 and May 6, 2026 — classified as 15 injuries.

The most frequently reported specific device problem is “Fracture” (3 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 15 most recent of 15 reports, in the reporter's own words as published by the FDA.

• InjuryMay 6, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT UNDERWENT REVISION KNEE SURGERY FOLLOWING A PERIPROSTHETIC FRACTURE OF THE TIBIA, DURING WHICH ALL PROSTHETIC COMPONENTS WERE REMOVED. APPROXIMATELY 25 DAYS POST-IMPLANTATION. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Periprosthetic fracture

  MAUDE report 25091781 ↗
• InjurySep 9, 2025Fracture; Fracture

  IT WAS REPORTED THAT THE PATIENT UNDERWENT REVISION SURGERY ON THE LEFT KNEE DUE TO THE FRACTURE OF BEARING TEN YEARS POST IMPLANTATION. DUE DILIGENCE IS IN PROGRESS FOR THIS COMPLAINT; TO DATE NO ADDITIONAL INFORMATION OR PRODUCT HAS BEEN RECEIVED.

  Patient problems: Insufficient Information

  MAUDE report 23003516 ↗
• InjuryAug 11, 2025Naturally Worn; Naturally Worn

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

  Patient problems: Insufficient Information

  MAUDE report 22772235 ↗
• InjuryFeb 16, 2024Fracture; Device Dislodged or Dislocated; Naturally Worn; Fracture; Device Dislodged or Dislocated; Naturally Worn

  IT WAS REPORTED THAT PATIENT UNDERWENT A UNI KNEE ARTHROPLASTY AND SUBSEQUENTLY THERE WAS A DISLOCATION OF THE MOBILE INLAY DURING A ROTATIONAL MOVEMENT OF THE LEFT KNEE JOINT. INTRAOPERATIVELY AN INLAY FRACTURE WAS DETECTED DURING REPLACEMENT SURGERY. DUE DILIGENCE IS IN PROGRESS FOR THIS COMPLAINT; TO DATE NO ADDITIONAL INFORMATION OR PRODUCT HAS BEEN RECEIVED.

  Patient problems: Failure of Implant; Joint Dislocation; Loss of Range of Motion; Pain

  MAUDE report 18720046 ↗
• InjuryDec 18, 2023Patient Device Interaction Problem; Patient Device Interaction Problem

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A UNI KNEE ARTHROPLASTY AND APPROXIMATELY 7 MONTHS LATER A REVISION SURGERY WAS PERFORMED DUE TO THE FAILED IMPLANT ON TIBIAL SIDE. THERE WAS A VISIBLE CYST ABOUT THE SIZE OF A MARBLE TOWARD TO POSTERIOR ASPECT OF THE TIBIA THAT WAS MOSTLY CONTAINED. DUE DILIGENCE IS IN PROGRESS FOR THIS COMPLAINT; TO DATE NO ADDITIONAL INFORMATION OR PRODUCT HAS BEEN RECEIVED.

  Patient problems: Cyst(s); Failure of Implant

  MAUDE report 18343140 ↗
• InjuryJul 17, 2023Unstable; Unstable

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

  Patient problems: Ambulation or Postural Difficulties; Pain

  MAUDE report 17331394 ↗
• InjuryFeb 27, 2023Fracture; Fracture

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A BEARING REVISION DUE TO FRACTURE WITHOUT ADEQUATE TRAUMA, APPROXIMATELY 15 YEARS POST-OP.

  Patient problems: Failure of Implant

  MAUDE report 16442278 ↗
• InjurySep 28, 2022Degraded; Degraded

  IT WAS REPORTED THAT PATIENT UNDERWENT REVISION SURGERY DUE WEAR AND PAIN APPROXIMATELY ONE AND A HALF (1.5) YEAR POST OP. DUE DILIGENCE IS IN PROGRESS FOR THIS COMPLAINT; TO DATE NO ADDITIONAL INFORMATION OR PRODUCT HAS BEEN RECEIVED.

  Patient problems: Pain

  MAUDE report 15500406 ↗
• InjuryJun 1, 2022Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION SURGERY DUE TO UNKNOWN REASON, APPROXIMATELY 3 YEARS POST-OP. DUE DILIGENCE IS IN PROGRESS FOR THIS COMPLAINT; TO DATE NO ADDITIONAL INFORMATION OR PRODUCT HAS BEEN RECEIVED.

  Patient problems: Insufficient Information

  MAUDE report 14560645 ↗
• InjuryApr 26, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED, THAT: THERE WAS A REVISION DUE TO THE OXFORD WARRANTY. PATIENT OUTCOME: REVISION. NO DELAY.

  Patient problems: Failure of Implant

  MAUDE report 14202144 ↗
• InjuryJul 7, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A PATIENT UNDERWENT AN INITIAL LEFT KNEE ARTHROPLASTY ON (B)(6)2017. SUBSEQUENTLY, THE OXFORD BEARING WAS REVISED ON (B)(6)2017 DUE TO UNKNOWN REASON. NO ADDITIONAL INFORMATION IS AVAILABLE. THIS REPORT IS BASED ON ALLEGATIONS SET FORTH IN PATIENTS NOTICE AND THE ALLEGATIONS THERE IN ARE UNVERIFIED.

  Patient problems: Insufficient Information

  MAUDE report 12126612 ↗
• InjuryJul 1, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED A PATIENT UNDERWENT AN INITIAL LEFT KNEE ARTHROPLASTY ON (B)(6), 2017. SUBSEQUENTLY, WAS REVISED DUE TO PAIN AND HEMARTHROSIS ON (B)(6), 2021.

  Patient problems: Pain

  MAUDE report 12098330 ↗
• InjuryFeb 28, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL LEFT KNEE ARTHROPLASTY. SUBSEQUENTLY, A REVISION DUE TO UNKNOWN REASONS WAS PERFORMED.

  Patient problems: Pain

  MAUDE report 9768515 ↗
• InjuryJul 9, 2019Insufficient Device Problem Information; Appropriate Device Problem Term/Code Not Available; Insufficient Device Problem Information; Appropriate Device Problem Term/Code Not Available

  IT WAS REPORTED BY A SALES REPRESENTATIVE THAT A SURGEON IMPLANTED A LEFT BEARING, INSTEAD OF THE RIGHT. THERE HAS BEEN NO FURTHER ACTION TAKEN ON THIS INCIDENT.

  Patient problems: No Information

  MAUDE report 8771144 ↗
• InjuryJun 21, 2019Unsealed Device Packaging; Unsealed Device Packaging

  IT WAS REPORTED BY THE HOSPITAL THAT WHEN REMOVING THE PEEL-OFF SEAL IT WAS RECOGNIZED THAT A PART OF ABOUT 1 CM WASN'T WELDED WITH THE PLASTIC PACKAGING. SUBSEQUENTLY, THE STERILITY COULD NOT BE ENSURED, THEREFORE THE IMPLANT WASN'T USED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8721951 ↗

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-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-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-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-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-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-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-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-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-1163-2017 · Jan 5, 2016 · Terminated
  Oxford Partial Knee System Left Medial Tibial Trial Tray Size D 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-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-1157-2017 · Jan 5, 2016 · Terminated
  Oxford Partial Knee System Left Medial Tibial Trial Tray Size F 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-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-1161-2017 · Jan 5, 2016 · Terminated
  Oxford Partial Knee System Left Medial Tibial Trial Tray Size E Product Usage: Instruments for use with the Oxford Uni Partial Knee System

…and 7 more.