International safety notice
Recall for PERIMOUNT aortic, PERIMOUNT Plus, PERIMOUNT Magna Ease valves, Edwards Lifesciences
Germany / BfArM · DEU · Aug 5, 2009
Key facts
| Title | Recall for PERIMOUNT aortic, PERIMOUNT Plus, PERIMOUNT Magna Ease valves, Edwards Lifesciences |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | PERIMOUNT aortic, PERIMOUNT Plus, PERIMOUNT Magna Ease valves, Edwards Lifesciences |
| Manufacturer | Recall for PERIMOUNT aortic, PERIMOUNT Plus, PERIMOUNT Magna Ease valves, Edwards Lifesciences |
| Models | 888972, 1594650, 250.2500, 1673318, 1709252, 1650496, 1680383, 6900P27C, 1547537, 949.250.2525, 92614, 949.250.2500 and 11 more |
| Date | Aug 5, 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