International safety notice
Urgent Field Safety Notice for ANGIOGUARD RX/XP Emboli Capture Guidewire System by Cordis Corporation
Germany / BfArM · DEU · Mar 29, 2023
Key facts
| Title | Urgent Field Safety Notice for ANGIOGUARD RX/XP Emboli Capture Guidewire System by Cordis Corporation |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | ANGIOGUARD RX/XP Emboli Capture Guidewire System |
| Manufacturer | Cordis Corporation |
| Models | 701814RE, 35265654, 35265641, 401814RM, 501814RMC, 35265344, 501814REC, 35264806, 35264216, 35265335, 35265648, 35265342 and 53 more |
| Date | Mar 29, 2023 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No 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