International safety notice
PRECISE PRO RX™ Carotid Stent System; Ver códigos de producto afectados en la Tabla 1 de la nota de aviso de la empresa
Spain / AEMPS · ESP · Feb 25, 2021
Key facts
| Title | PRECISE PRO RX™ Carotid Stent System; Ver códigos de producto afectados en la Tabla 1 de la nota de aviso de la empresa |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | PRECISE PRO RX™ Carotid Stent System; Ver códigos de producto afectados en la Tabla 1 de la nota de aviso de la empresa |
| Manufacturer | Cordis Corporation, Estados Unidos |
| Models | 17945245, 17931760, 17942802, 17937808, 17936917, 17910550, 17912282, 17961561, 17913483, 17925700, 17909817, 17962540 and 141 more |
| Event type | Safety Notice |
| Date | Feb 25, 2021 |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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