International safety notice
Biosense Webster recalls the Celsius® ThermoCool® and NaviStar® ThermoCool® irrigated ablation catheters
Germany / BfArM · DEU · Sep 19, 2005
Key facts
| Title | Biosense Webster recalls the Celsius® ThermoCool® and NaviStar® ThermoCool® irrigated ablation catheters |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Biosense Webster recalls the Celsius® ThermoCool® and NaviStar® ThermoCool® irrigated ablation catheters |
| Manufacturer | Biosense Webster recalls the Celsius® ThermoCool® and NaviStar® ThermoCool® irrigated ablation catheters |
| Models | 210-0057600-34, 34G-17M, 35R-57R, 634533, 35Q-17Q, 34G-37M, 35Q-53R, 35Q-57Q, 34H-17M, 34G-27M, 425-967-580, 35Q-37Q and 14 more |
| Date | Sep 19, 2005 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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