International safety notice

Urgent field safety notice for V-PRO 1 / V-PRO 1 Plus / V-PRO maX Low Temperature Sterilization Systems, STERIS Corporation

Germany / BfArM · DEU · Jun 13, 2016

Key facts

Title Urgent field safety notice for V-PRO 1 / V-PRO 1 Plus / V-PRO maX Low Temperature Sterilization Systems, STERIS Corporation
Regulator Germany / BfArM
Country DEU
Brand V-PRO 1 / V-PRO 1 Plus / V-PRO maX Low Temperature Sterilization Systems, STERIS Corporation
Manufacturer Urgent field safety notice for V-PRO 1 / V-PRO 1 Plus / V-PRO maX Low Temperature Sterilization Systems, STERIS Corporation
Models 1-800-548-4873, 392-7375
Date Jun 13, 2016
Regulator page bfarm.de

At a glance

  • No Recall
  • No 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

Browse all International device safety notices