International safety notice
Safety Notice concerning a corrective action of the Lifepak 500 automated external defibrillator, Medtronic Physio-Control
Germany / BfArM · DEU · Jul 4, 2011
Key facts
| Title | Safety Notice concerning a corrective action of the Lifepak 500 automated external defibrillator, Medtronic Physio-Control |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Safety Notice concerning a corrective action of the Lifepak 500 automated external defibrillator, Medtronic Physio-Control |
| Manufacturer | Safety Notice concerning a corrective action of the Lifepak 500 automated external defibrillator, Medtronic Physio-Control |
| Models | LIFEPAK®500AUTOMATEDEXTERNALDEFIBRILLATOR, LP500READINESSDISPLAY, PRODUCT-SUPPORT.ASPX?ID=558, YESDEVICEREADINESSHASBEENCHECKEDANDVERIFIEDWITHINTHELAST30DAYS, PRODUCTSUPPORT.ASPX?ID=558, JUNE2011, FA521, LIFEPAK500AEDOPERATINGINSTRUCTIONS.ACOPYOFTHEOPERATINGINSTRUCTIONSCANBEDOWNLOADED |
| Date | Jul 4, 2011 |
| 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