International safety notice
Corrective action for the Zeus Infinity Empowered (IE) anaesthesia workstation with integrated patient monitoring, Dräger Medical GmbH
Germany / BfArM · DEU · May 30, 2014
Key facts
| Title | Corrective action for the Zeus Infinity Empowered (IE) anaesthesia workstation with integrated patient monitoring, Dräger Medical GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Zeus Infinity Empowered (IE) anaesthesia workstation with integrated patient monitoring, Dräger Medical GmbH |
| Manufacturer | Corrective action for the Zeus Infinity Empowered (IE) anaesthesia workstation with integrated patient monitoring, Dräger Medical GmbH |
| Models | NOLADE21, 23558, FORSP02, COBADEFF230, 53-55, 882-0, SP02-LOW, 23542, THAN10, 882-2080, DE813745277 |
| Date | May 30, 2014 |
| 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