International safety notice
Corrective action for the Philips HeartStart MRx Monitor/Defibrillator, Philips Healthcare
Germany / BfArM · DEU · Dec 15, 2014
Key facts
| Title | Corrective action for the Philips HeartStart MRx Monitor/Defibrillator, Philips Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Philips HeartStart MRx Monitor/Defibrillator, Philips Healthcare |
| Manufacturer | Corrective action for the Philips HeartStart MRx Monitor/Defibrillator, Philips Healthcare |
| Models | US00543158, US00543166, US00101159, US00543223, US00543161, US00535118, M3536A, US00328464, US00543104, US00328432, US00326834, US00328442 and 25 more |
| Date | Dec 15, 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