International safety notice

Aesculap

United Kingdom / MHRA · GBR · Mar 6, 2017

Key facts

Title Aesculap
Regulator United Kingdom / MHRA
Country GBR
Brand MINOP INVENT 30DG TROCAR D8.3MM L150MM
Manufacturer Aesculap
Models FH620R, 95-2182, 7461-95, 78532, DE812160059, 95-1599, 14614, DEUTDESS653, 95-1555, 65109852, 726261
Event type Recall, Safety Notice
Action type Field safety notice
Date Mar 6, 2017
Regulator page gov.uk

At a glance

  • Yes 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