International safety notice

Biomet (Zimmer)

United Kingdom / MHRA · GBR · Apr 10, 2019

Key facts

Title Biomet (Zimmer)
Regulator United Kingdom / MHRA
Country GBR
Brand T7 Driver AO
Manufacturer Biomet (Zimmer)
Models REV.3, 110018531, CF04108, 2019-00046, 2.12-1, 110018541, ZFA2019-00046, CP04102
Event type Safety Notice
Action type Field safety notice
Medical specialty Orthopaedics, Radiology
Date Apr 10, 2019
Regulator page gov.uk

At a glance

  • No Recall
  • Yes Field safety notice
  • 1–9 Matching device models in FDA data
  • 1–9 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