International safety notice
Urgent Safety Notice for the Philips HeartStart XL+ Defibrillator/Monitor, Philips Healthcare
Germany / BfArM · DEU · May 19, 2014
Key facts
| Title | Urgent Safety Notice for the Philips HeartStart XL+ Defibrillator/Monitor, Philips Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Philips HeartStart XL+ Defibrillator/Monitor, Philips Healthcare |
| Manufacturer | Urgent Safety Notice for the Philips HeartStart XL+ Defibrillator/Monitor, Philips Healthcare |
| Models | US61201722, USO1202990, USD1308424, US91202514, USD1203968, US21303980, US61305451, FSN86100139, US61306138, US21410563, US11201096, US21201187 and 49 more |
| Date | May 19, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 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