International safety notice
Recall for CardioVations EndoClamp Aortic Catheter, Edwards Lifesciences
Germany / BfArM · DEU · Jan 7, 2009
Key facts
| Title | Recall for CardioVations EndoClamp Aortic Catheter, Edwards Lifesciences |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | CardioVations EndoClamp Aortic Catheter, Edwards Lifesciences |
| Manufacturer | Recall for CardioVations EndoClamp Aortic Catheter, Edwards Lifesciences |
| Models | 007026, 31.412.47.66.99=, MS1007022, 562406, 007022, MS0208036, EC1001, MS0208019, 569135, MS0508040, MS1007026, MS0208020 and 12 more |
| Date | Jan 7, 2009 |
| 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