International safety notice
Dispositivo trombolítico percutáneo Arrow-Trerotola™ Over-The-Wire PTD Kit®. Ver códigos de afectados en la nota de aviso de la empresa
Spain / AEMPS · ESP · Oct 7, 2021
Key facts
| Title | Dispositivo trombolítico percutáneo Arrow-Trerotola™ Over-The-Wire PTD Kit®. Ver códigos de afectados en la nota de aviso de la empresa |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Dispositivo trombolítico percutáneo Arrow-Trerotola™ Over-The-Wire PTD Kit®. Ver códigos de afectados en la nota de aviso de la empresa |
| Manufacturer | Arrow International LLC, Estados Unidos |
| Models | 13F20F0231, 13C21E1991, 13C21A0855, 13F21F1187, 13C19K2024, PT-03009, 13F21F1189, 13F20H0756, 14C20J1453, 13C20G0230, 13C21B1533, PT-65709-HFS and 141 more |
| Event type | Safety Notice |
| Date | Oct 7, 2021 |
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