International safety notice
Catéter Fogarty para atrioseptostomía por dilatación con balón Miller, modelo 830515F y Catéter Fogarty para atrioseptostomía por dilatación, modelo 830705F.
Spain / AEMPS · ESP · May 14, 2019
Key facts
| Title | Catéter Fogarty para atrioseptostomía por dilatación con balón Miller, modelo 830515F y Catéter Fogarty para atrioseptostomía por dilatación, modelo 830705F. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Catéter Fogarty para atrioseptostomía por dilatación con balón Miller, modelo 830515F y Catéter Fogarty para atrioseptostomía por dilatación, modelo 830705F. |
| Manufacturer | Edwards Lifesciences LLC, Estados Unidos. |
| Models | 34-916, 52065, 31-499-377388, 2019-252, 830515F, 91.822.52.89, 28022, 46980, 830705F |
| Event type | Safety Notice |
| Date | May 14, 2019 |
At a glance
- No Recall
- Yes 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