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Oxford Partial Knee System 32-420376

by Biomet Uk Ltd

Oxford Partial Knee System 32-420376 is a Class III device made by Biomet Uk Ltd, approved under FDA PMA P010014 on 21 Apr 2004 and listed in FDA GUDID since 29 Aug 2014 (UDI-DI 05019279483464), active as of 22 Oct 2026. 14 FDA recalls are linked to it.

Active United States. Also listed in GUDID (US).

PMA

Valid until

No expiry

PMA approval is not time-limited

FDA recalls

None ongoing

22 closed

Documents

PMA P010014

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05019279483464 UDI-DI Date29 Aug 2014ListedStatusListed GUDID: in commercial distribution
United StatesFDA PMAAPPR from GUDID Approved NumberP010014 Date21 Apr 2004DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA PMA P010014 decided 21 Apr 2004 Active
  • FDA GUDID UDI-DI 05019279483464 listed 29 Aug 2014 Listed

Recalls

22 recalls · FDA

  • 20 recalls, same reason

    • Terminated Z-1153-2017 FDA Class II initiated 5 Jan 2016 on shared PMA P010014
    • Terminated Z-1168-2017 FDA Class II initiated 5 Jan 2016 on shared PMA P010014
    • Terminated Z-1162-2017 FDA Class II initiated 5 Jan 2016
    • Terminated Z-1152-2017 FDA Class II initiated 5 Jan 2016 on shared PMA P010014
    • Terminated Z-1159-2017 FDA Class II initiated 5 Jan 2016
    • Terminated Z-1170-2017 FDA Class II initiated 5 Jan 2016 on shared PMA P010014
    • Terminated Z-1165-2017 FDA Class II initiated 5 Jan 2016
    • Terminated Z-1173-2017 FDA Class II initiated 5 Jan 2016
    • Terminated Z-1158-2017 FDA Class II initiated 5 Jan 2016
    • Terminated Z-1172-2017 FDA Class II initiated 5 Jan 2016
    • Terminated Z-1161-2017 FDA Class II initiated 5 Jan 2016
    • Terminated Z-1169-2017 FDA Class II initiated 5 Jan 2016 on shared PMA P010014
    • Terminated Z-1157-2017 FDA Class II initiated 5 Jan 2016
    • Terminated Z-1163-2017 FDA Class II initiated 5 Jan 2016
    • Terminated Z-1155-2017 FDA Class II initiated 5 Jan 2016 on shared PMA P010014
    • Terminated Z-1156-2017 FDA Class II initiated 5 Jan 2016
    • Terminated Z-1154-2017 FDA Class II initiated 5 Jan 2016 on shared PMA P010014
    • Terminated Z-1164-2017 FDA Class II initiated 5 Jan 2016
    • Terminated Z-1160-2017 FDA Class II initiated 5 Jan 2016
    • Terminated Z-1171-2017 FDA Class II initiated 5 Jan 2016

    Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.

    • Terminated Z-2698-2011 FDA Unclassified (pre-2012) initiated 22 Apr 2011 on shared PMA P010014

    This recall was initiated due to a customer complaint which reported that while peeling off the Tyvek lid on the blister pack, very little effort was required to remove it and this could lead to contamination of the device.

    • Terminated Z-0962-2009 FDA Unclassified (pre-2012) initiated 19 Dec 2008

    Packages labeled as "right" actually contain a "left" component.

Recalls on a shared submission name another device cleared under the same FDA submission as this one.

Timeline

24 dated events

  1. Recall initiated FDA recalls Z-1161-2017
  2. Recall initiated FDA recalls Z-1169-2017
  3. Recall initiated FDA recalls Z-1157-2017
  4. Recall initiated FDA recalls Z-1163-2017
  5. Recall initiated FDA recalls Z-1155-2017
  6. Recall initiated FDA recalls Z-1156-2017
  7. Recall initiated FDA recalls Z-1154-2017
  8. Recall initiated FDA recalls Z-1164-2017
  9. Recall initiated FDA recalls Z-1160-2017
  10. Recall initiated FDA recalls Z-1171-2017

14 earlier events are in the sections above.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA PMA Active

Specification

GUDID

Trade name
Oxford Partial Knee System
Generic name
Knee tibia prosthesis trial, reusable
Model / Ref / Catalog
32-420376
Primary DI / UDI-DI
05019279483464
PMA number
FDA product code
NRA
GMDN term
Knee tibia prosthesis trial, reusable
Device class
Class III
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Knee tibia prosthesis trial, reusable

Cleared under the same submission (P010014)

and 8 more cleared under P010014

Similar devices in this category

Other devices filed under Knee tibia prosthesis trial, reusable.

Other devices from Biomet Uk Ltd

See all devices from Biomet Uk Ltd →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)