International safety notice

Stanmore

United Kingdom / MHRA · GBR · Jan 20, 2017

Key facts

Title Stanmore
Regulator United Kingdom / MHRA
Country GBR
Brand Custom-made Medical Device - Glenoid Shell & Proximal Humeral Replacement
Manufacturer Stanmore
Models 20391
Event type Safety Notice
Action type Field safety notice
Date Jan 20, 2017
Regulator page gov.uk

At a glance

  • No Recall
  • Yes Field safety notice

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

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