International safety notice

Zimmer Biomet

United Kingdom / MHRA · GBR · Feb 24, 2017

Key facts

Title Zimmer Biomet
Regulator United Kingdom / MHRA
Country GBR
Brand Various Polyethylene Implants
Manufacturer Zimmer Biomet
Models 456260, 293190, CP753461, 577290, 605260, 371770, 605350, 189080, XL-200144, 668260, 347970, 159556 and 2063 more
Event type Recall, Safety Notice
Action type Field safety notice
Date Feb 24, 2017
Regulator page gov.uk

At a glance

  • Yes Recall
  • Yes Field safety notice
  • 100–999 Matching device models in FDA data
  • 100–999 Matching catalog numbers in FDA data

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

Browse all International device safety notices