International safety notice

Urgent Field Safety Notice for Zeus/ Zeus kit C500/ Zeus IE with DIVA Sevoflurane by Drägerwerk AG & Co. KGaA

Germany / BfArM · DEU · May 12, 2022

Key facts

Title Urgent Field Safety Notice for Zeus/ Zeus kit C500/ Zeus IE with DIVA Sevoflurane by Drägerwerk AG & Co. KGaA
Regulator Germany / BfArM
Country DEU
Brand Zeus/ Zeus kit C500/ Zeus IE with DIVA Sevoflurane
Manufacturer Drägerwerk AG & Co. KGaA
Models ASNL-0030, DE135082211, ASLM-0001, ASNL-0008, ASML-0011, ASLN-0029, ASNA-0028, ASNM-0046, ASNE-0051, ASNM-0054, ASPM-0053, ASPB-0003 and 475 more
Date May 12, 2022
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 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