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Biomet Uk Ltd devices, product family

by Biomet Uk Ltd 14 variants Basic UDI-DI 889024XJLC

Shared by every variant

Manufacturer
Biomet Uk Ltd(14)
Basic UDI-DI
889024XJLC
Risk class
Class III
Legislation
—
EMDN category
—
Market status
14 on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 889024XJLC.

Certificates

1 certificate naming this Basic UDI-DI · EUDAMED

  • MDR 754277 Technical documentation · refdata.applicable-legislation.mdr supplemented
    Notified body 2797 · holder Biomet UK Ltd · issued 11 Aug 2026 · expires 6 Nov 2027

Recalls

20 recalls · FDA

  • Z-1153-2017 Class II · terminated · 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.
  • Z-1168-2017 Class II · terminated · 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.
  • Z-1162-2017 Class II · terminated · 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.
  • Z-1152-2017 Class II · terminated · 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.
  • Z-1159-2017 Class II · terminated · 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.
  • Z-1170-2017 Class II · terminated · 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.
  • Z-1165-2017 Class II · terminated · 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.
  • Z-1173-2017 Class II · terminated · 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.
  • Z-1158-2017 Class II · terminated · 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.
  • Z-1172-2017 Class II · terminated · 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.
  • Z-1161-2017 Class II · terminated · 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.
  • Z-1169-2017 Class II · terminated · 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.
  • Z-1157-2017 Class II · terminated · 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.
  • Z-1163-2017 Class II · terminated · 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.
  • Z-1155-2017 Class II · terminated · 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.
  • Z-1156-2017 Class II · terminated · 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.
  • Z-1154-2017 Class II · terminated · 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.
  • Z-1164-2017 Class II · terminated · 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.
  • Z-1160-2017 Class II · terminated · 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.
  • Z-1171-2017 Class II · terminated · 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.

Recalls matched to the 14 devices listed on this page; other pages of the family can carry others.

Variants

14 devices · page 1 of 1

Variants of Biomet Uk Ltd devices, Basic UDI-DI 889024XJLC
UDI-DISize and differences
Oxford Partial Knee System 154719 154719 / 15471905019279388851 —On the market
Oxford Partial Knee System 154720 154720 / 15472005019279388868 —On the market
Oxford Partial Knee System 154721 154721 / 15472105019279388875 —On the market
Oxford Partial Knee System 154722 154722 / 15472205019279388882 —On the market
Oxford Partial Knee System 154723 154723 / 15472305019279388899 —On the market
Oxford Partial Knee System 154724 154724 / 15472405019279388905 —On the market
Oxford Partial Knee System 154725 154725 / 15472505019279388912 —On the market
Oxford Partial Knee System 154726 154726 / 15472605019279388929 —On the market
Oxford Partial Knee System 154727 154727 / 15472705019279388936 —On the market
Oxford Partial Knee System 154775 154775 / 15477505019279389155 —On the market
Oxford Partial Knee System 154776 154776 / 15477605019279389162 —On the market
Oxford Partial Knee System 159531 159531 / 15953105019279783137 —On the market
Oxford Partial Knee System 159532 159532 / 15953205019279783144 —On the market
Oxford® Partial Knee System 154718 154718 / 15471805019279388844 —On the market