International safety notice
Recall for Internal Defibrillation Paddles and Handles without discharge control for use with LIFEPAK 9 or LIFEPAK 9P, Medtronic
Germany / BfArM · DEU · Mar 19, 2009
Key facts
| Title | Recall for Internal Defibrillation Paddles and Handles without discharge control for use with LIFEPAK 9 or LIFEPAK 9P, Medtronic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | use with LIFEPAK 9 or LIFEPAK 9P, Medtronic |
| Manufacturer | Recall for Internal Defibrillation Paddles and Handles without discharge control for use with LIFEPAK 9 or LIFEPAK 9P, Medtronic |
| Models | 802154-10, 800441-03, LIFEPAK®9, 800441, 800441-36, 802154, FA424, THRU-39 |
| Date | Mar 19, 2009 |
| 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