International safety notice
Bifurcación endoprótesis vascular-ilíaca Zenith® Branch (ZBIS), Endoprótesis vascular de rama lateral ilíaca bifurcada (Producto a medida). Ver números de referencia afectados en la nota de aviso de la empresa.
Spain / AEMPS · ESP · Apr 21, 2023
Key facts
| Title | Bifurcación endoprótesis vascular-ilíaca Zenith® Branch (ZBIS), Endoprótesis vascular de rama lateral ilíaca bifurcada (Producto a medida). Ver números de referencia afectados en la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Bifurcación endoprótesis vascular-ilíaca Zenith® Branch (ZBIS), Endoprótesis vascular de rama lateral ilíaca bifurcada (Producto a medida). Ver números de referencia afectados en la nota de aviso de la empresa. |
| Manufacturer | William A. Cook Australia Pty Ltd, Australia. |
| Models | A1127154, A1075850, A1067505, A1100435, A1100151, A1101053, A1127205, A1090937, A1092037, A1057901, A1073738, A1125487 and 242 more |
| Event type | Safety Notice |
| Date | Apr 21, 2023 |
At a glance
- No Recall
- Yes Field safety notice
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