International safety notice
• Válvula aórtica transcatéter CoreValve™ Evolut™ R • Válvula aórtica transcatéter CoreValve™ Evolut™ PRO Ver modelos afectados en la nota de aviso de la empresa
Spain / AEMPS · ESP · Oct 30, 2020
Key facts
| Title | • Válvula aórtica transcatéter CoreValve™ Evolut™ R • Válvula aórtica transcatéter CoreValve™ Evolut™ PRO Ver modelos afectados en la nota de aviso de la empresa |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | • Válvula aórtica transcatéter CoreValve™ Evolut™ R • Válvula aórtica transcatéter CoreValve™ Evolut™ PRO Ver modelos afectados en la nota de aviso de la empresa |
| Manufacturer | Medtronic CoreValve LLC, EEUU |
| Models | 28022, FA935, 63304, EVOLUTR-34, EVOLUTR-26, EVOLUTR-23, EVOLUTR-29, EVOLUTPRO-26, 28050, EVOLUTPRO-29, EVOLUTPRO-23, 91.822.52.89 and 1 more |
| Event type | Safety Notice |
| Date | Oct 30, 2020 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models 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