International safety notice
Corrective action for the IntelliVue Patient Monitors MP2, X2, MP5/MP5T and MP20-50 containing battery operation, Philips Healthcare
Germany / BfArM · DEU · May 30, 2014
Key facts
| Title | Corrective action for the IntelliVue Patient Monitors MP2, X2, MP5/MP5T and MP20-50 containing battery operation, Philips Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the IntelliVue Patient Monitors MP2, X2, MP5/MP5T and MP20-50 containing battery operation, Philips Healthcare |
| Manufacturer | Corrective action for the IntelliVue Patient Monitors MP2, X2, MP5/MP5T and MP20-50 containing battery operation, Philips Healthcare |
| Models | M8003A, M8002A, M8004A, M8105A, M4605A, M8102A, M4607A, FSN86201525A, M3002A, M8001A, M8105AT |
| Date | May 30, 2014 |
| 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