International safety notice
Biosense Webster
United Kingdom / MHRA · GBR · Apr 6, 2020
Key facts
| Title | Biosense Webster |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | PENTARAY® NAV CATHETER; PENTARAY® NAV eco CATHETER |
| Manufacturer | Biosense Webster |
| Models | 1-800-729-9010, D128210, D128209, D128202, 0.0008, D128206, D128203, D128212, D128211, D128201, D128208, D128205 and 3 more |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | Apr 6, 2020 |
| Regulator page | gov.uk |
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