Oxford® Partial Knee System, product family

Manufacturer

Biomet Uk Ltd(14)

Basic UDI-DI

889024XMLJ

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 889024XMLJ.

• MDR 754285 ·Technical documentation · refdata.applicable-legislation.mdr ·supplemented
  Notified body 2797 · holder Biomet UK Ltd · issued 9 Sep 2026 · expires 6 Nov 2027

• 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.