International safety notice
Cordis
United Kingdom / MHRA · GBR · Aug 23, 2019
Key facts
| Title | Cordis |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Cordis® POWERFLEX® PRO PTA Dilatation Catheter |
| Manufacturer | Cordis |
| Models | 82144947, 82144115, 82144499, 4400602S, 82144617, 82144604, 82144141, CORDIS20180906-OUS, 4400508S, 82148810, 4400604S, 4400308S and 4 more |
| Event type | Recall, Safety Notice |
| Action type | Field safety notice |
| Date | Aug 23, 2019 |
| Regulator page | gov.uk |
At a glance
- Yes Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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