Oxford Partial Knee System 159543Recalls & reported problems
Biomet Uk Ltd · Anatomic Meniscal Bearing Left Medial · Class 3 · Implant
All models of Oxford Partial Knee System (92)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05019279785896), received between Oct 7, 2019 and Jun 11, 2020 — classified as 2 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).
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
Device problems
- Device Dislodged or Dislocated1
- Insufficient Device Problem Information1
Patient problems
- Joint Dislocation1
- No Information1
- Pain1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJun 11, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT PATIENT WHO UNDERWENT UKA WITH OXFORD ON (B)(6) 2016 HAD A PAIN ON OPERATED KNEE AND WENT TO SEE A DOCTOR. AT THE DIAGNOSIS, BACKWARD DISLOCATION OF THE BEARING (THICKNESS 6MM) WAS OBSERVED BY X-RAY ON (B)(6) 2020. A REVISION WAS IMPLEMENTED TO REPLACE THE BEARING WITH THICKER ONE (THICKNESS 9MM) ON (B)(6).
Patient problems: Joint Dislocation; Pain
MAUDE report 10143103 ↗InjuryOct 7, 2019Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED THAT A PATIENT UNDERWENT PARTIAL KNEE REVISION OF THE FEMORAL COMPONENT AND BEARING DUE TO AN UNKNOWN REASON. SUBSEQUENTLY, A SECOND REVISION TOOK PLACE TO A TOTAL KNEE DUE TO AN UNKNOWN REASON.
Patient problems: No Information
MAUDE report 9160814 ↗
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-1158-2017 · Jan 5, 2016 · TerminatedOxford Partial Knee System Right Medial Tibial Trial Tray Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System
- Z-1159-2017 · Jan 5, 2016 · TerminatedOxford 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 · TerminatedOxford Partial Knee System Right Medial Tibial Trial Tray Size E Product Usage: Instruments for use with the Oxford Uni Partial Knee System
- Z-1171-2017 · Jan 5, 2016 · TerminatedOxford Partial Knee System Phase 3 Tibial Template Right Medial Size D Product Usage: Instruments for use with the Oxford Uni Partial Knee System
- Z-1161-2017 · Jan 5, 2016 · TerminatedOxford Partial Knee System Left Medial Tibial Trial Tray Size E Product Usage: Instruments for use with the Oxford Uni Partial Knee System
- Z-1154-2017 · Jan 5, 2016 · TerminatedOxford Unicompartmental Knee Phase 3 Tibial Impactor Product Usage: Instruments for use with the Oxford Uni Partial Knee System
- Z-1169-2017 · Jan 5, 2016 · TerminatedOxford 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 · TerminatedOxford Partial Knee System Right Medial Tibial Trial Tray Size F Product Usage: Instruments for use with the Oxford Uni Partial Knee System
- Z-1170-2017 · Jan 5, 2016 · TerminatedOxford Unicompartmental Knee Phase 3 Shim Size 1 Product Usage: Instruments for use with the Oxford Uni Partial Knee System
- Z-1152-2017 · Jan 5, 2016 · TerminatedOxford Knee System Tibial Resector Body Tube & Guides Product Usage: Instruments for use with the Oxford Uni Partial Knee System
- Z-1173-2017 · Jan 5, 2016 · TerminatedOxford Partial Knee System Phase 3 Tibial Template Right Medial Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System
- Z-1162-2017 · Jan 5, 2016 · TerminatedOxford Partial Knee System Right Medial Tibial Trial Tray Size D Product Usage: Instruments for use with the Oxford Uni Partial Knee System
- Z-1172-2017 · Jan 5, 2016 · TerminatedOxford Partial Knee System Phase 3 Tibial Template Left Medial Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System
- Z-1155-2017 · Jan 5, 2016 · TerminatedOxford Partial Knee System Phase 3 Tibial Template Right Medial Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System
- Z-1165-2017 · Jan 5, 2016 · TerminatedOxford Partial Knee System Right Medial Tibial Trial Tray Size C Oxford Partial Knee System Left Medial Tibial Trial Tray Size C
…and 7 more.
Other Prosthesis, Knee, Femorotibial, Unicompartmental, Semi-Constrained, Metal/Polymer, Mobile Bearing devices
- Oxford Partial Knee System 159575Biomet Uk Ltd · Prosthesis, Knee, Femorotibial, Unicompartmental, Semi-Constrained, Metal/Polymer, Mobile Bearing1 recall32 reports
- Oxford Partial Knee System 161468Biomet Uk Ltd · Prosthesis, Knee, Femorotibial, Unicompartmental, Semi-Constrained, Metal/Polymer, Mobile Bearing1 death69 reports
- Oxford Partial Knee System 161469Biomet Uk Ltd · Prosthesis, Knee, Femorotibial, Unicompartmental, Semi-Constrained, Metal/Polymer, Mobile Bearing65 reports
- Oxford Partial Knee System 154722Biomet Uk Ltd · Prosthesis, Knee, Femorotibial, Unicompartmental, Semi-Constrained, Metal/Polymer, Mobile Bearing35 reports
- Oxford Partial Knee System 159547Biomet Uk Ltd · Prosthesis, Knee, Femorotibial, Unicompartmental, Semi-Constrained, Metal/Polymer, Mobile Bearing33 reports
- Oxford® Partial Knee System 32-422097Biomet Uk Ltd · Prosthesis, knee, femorotibial, unicompartmental, semi-constrained, metal/polymer, mobile bearing32 reports
- Oxford Partial Knee System 154723Biomet Uk Ltd · Prosthesis, Knee, Femorotibial, Unicompartmental, Semi-Constrained, Metal/Polymer, Mobile Bearing1 death32 reports
- Oxford Partial Knee System 161470Biomet Uk Ltd · Prosthesis, Knee, Femorotibial, Unicompartmental, Semi-Constrained, Metal/Polymer, Mobile Bearing26 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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