Oxford Partial Knee System 32-420382Recalls & reported problems
Biomet Uk Ltd · Phase 3 Trial Bearing · Class 3
All models of Oxford Partial Knee System (92)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05019279483891), received between Nov 17, 2021 and Oct 3, 2022 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fracture” (2 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 18, 2026.
Most reported problems
Device problems
- Fracture2
- Break1
- Material Integrity Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 3, 2022Fracture; Fracture
IT WAS REPORTED, THAT THE TRIAL BEARING CRACKED WHERE IT SCREWS INTO THE HANDLE. NO CONSEQUENCES OR IMPACT TO THE PATIENT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15526863 ↗MalfunctionNov 17, 2021Break; Fracture; Material Integrity Problem; Break; Fracture; Material Integrity Problem
IT WAS REPORTED THAT THE POLY TRIAL BEARING CRACKED AND IS LOOSE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12826547 ↗
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-1153-2017 · Jan 5, 2016 · TerminatedOxford Partial Knee System Femoral Slap Hammer Product Usage: Instruments for use with the Oxford Uni Partial Knee System
- Z-1164-2017 · Jan 5, 2016 · TerminatedOxford Partial Knee System Right Medial Tibial Trial Tray Size C 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-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-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-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-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-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-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-1168-2017 · Jan 5, 2016 · TerminatedOxford Unicompartmental Knee Phase 3 Shim Size 3 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-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
- 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-1157-2017 · Jan 5, 2016 · TerminatedOxford Partial Knee System Left Medial Tibial Trial Tray Size F Product Usage: Instruments for use with the Oxford Uni Partial Knee System
…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 154723Biomet Uk Ltd · Prosthesis, Knee, Femorotibial, Unicompartmental, Semi-Constrained, Metal/Polymer, Mobile Bearing1 death32 reports
- Oxford® Partial Knee System 32-422097Biomet Uk Ltd · Prosthesis, knee, femorotibial, unicompartmental, semi-constrained, metal/polymer, mobile bearing32 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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