International safety notice
Recall for EndoClamp Aortic Catheters, Edwards Lifesciences
Germany / BfArM · DEU · Oct 21, 2009
Key facts
| Title | Recall for EndoClamp Aortic Catheters, Edwards Lifesciences |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | EndoClamp Aortic Catheters, Edwards Lifesciences |
| Manufacturer | Recall for EndoClamp Aortic Catheters, Edwards Lifesciences |
| Models | 651862, 608375, 628961, 591423, 643171, 598990, 608379, 651860, 581130, 623151, 618753, 605844 and 25 more |
| Date | Oct 21, 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