International safety notice

Recall of catheters for intracranial pressure monitoring, Spiegelberg

Germany / BfArM · DEU · Jan 12, 2010

Key facts

Title Recall of catheters for intracranial pressure monitoring, Spiegelberg
Regulator Germany / BfArM
Country DEU
Brand intracranial pressure monitoring, Spiegelberg
Manufacturer Recall of catheters for intracranial pressure monitoring, Spiegelberg
Models 21079, FV534P, D-21079, 13.1.63, 49-40-790-178-10, 49-1714340911, 49-40-790, 49-40-790-17810, 13.1.53, 178-0, FV535P, 6937-7122 and 8 more
Date Jan 12, 2010
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 1–9 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

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