International safety notice
Catéter guía Sherpa Active Nx de 6F (ver modelos afectados en el apéndice A de la nota de aviso de la empresa)
Spain / AEMPS · ESP · Apr 23, 2019
Key facts
| Title | Catéter guía Sherpa Active Nx de 6F (ver modelos afectados en el apéndice A de la nota de aviso de la empresa) |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Catéter guía Sherpa Active Nx de 6F (ver modelos afectados en el apéndice A de la nota de aviso de la empresa) |
| Manufacturer | Medtronic Inc, Estados Unidos |
| Models | 2019-206, SA6AL20A, SA6LCBD, 51852, 28022, SA6CHAMP20K, SA6JL40D, SA6EBU35D, SA6IMASH, SA6LCBSHD, SA6RBU35SH, SA6RDCK and 48 more |
| Event type | Safety Notice |
| Date | Apr 23, 2019 |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 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