International safety notice
Field Safety Notice concerning External Sterilizable Defibrillation Hard Paddles used with Lifepak 9, Lifepak9P, Lifepak 12 and Lifepak 20/20e defibrillators, Medtronic Physio-Control
Germany / BfArM · DEU · Nov 3, 2010
Key facts
| Title | Field Safety Notice concerning External Sterilizable Defibrillation Hard Paddles used with Lifepak 9, Lifepak9P, Lifepak 12 and Lifepak 20/20e defibrillators, Medtronic Physio-Control |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Field Safety Notice concerning External Sterilizable Defibrillation Hard Paddles used with Lifepak 9, Lifepak9P, Lifepak 12 and Lifepak 20/20e defibrillators, Medtronic Physio-Control |
| Manufacturer | Field Safety Notice concerning External Sterilizable Defibrillation Hard Paddles used with Lifepak 9, Lifepak9P, Lifepak 12 and Lifepak 20/20e defibrillators, Medtronic Physio-Control |
| Models | FA412, 3009166-03, 800418-00, 3009166-XX, 800418-05, 804507-XX, LIFEPAK®9, 800418-XX |
| Date | Nov 3, 2010 |
| 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