International safety notice
Cordis Corporation
United Kingdom / MHRA · GBR · May 4, 2016
Key facts
| Title | Cordis Corporation |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Cordis PRECISE® PRO RX Nitinol Stent System |
| Manufacturer | Cordis Corporation |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | May 4, 2016 |
| Regulator page | gov.uk |
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