International safety notice

Batch Recall concerning Burr Hole Latex Free Probe Cover with Gel, Microtek Medical B.V. and Microtek Medical Malta Ltd.

Germany / BfArM · DEU · Aug 12, 2013

Key facts

Title Batch Recall concerning Burr Hole Latex Free Probe Cover with Gel, Microtek Medical B.V. and Microtek Medical Malta Ltd.
Regulator Germany / BfArM
Country DEU
Brand Batch Recall concerning Burr Hole Latex Free Probe Cover with Gel, Microtek Medical B.V. and Microtek Medical Malta Ltd.
Manufacturer Batch Recall concerning Burr Hole Latex Free Probe Cover with Gel, Microtek Medical B.V. and Microtek Medical Malta Ltd.
Models D120651, 0121511, D102701, DA100061, 0121371, DI11651, 126611, 12661, 0101881, D101931, 130311, 092431 and 145 more
Date Aug 12, 2013
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 10–99 Matching device models in FDA data
  • 10–99 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