International safety notice
Corrective action of the Lifepak 500 automated external defibrillators from Medtronic
Germany / BfArM · DEU · Jun 27, 2007
Key facts
| Title | Corrective action of the Lifepak 500 automated external defibrillators from Medtronic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Corrective action of the Lifepak 500 automated external defibrillators from Medtronic |
| Manufacturer | Corrective action of the Lifepak 500 automated external defibrillators from Medtronic |
| Models | LP500 |
| Date | Jun 27, 2007 |
| 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