International safety notice
Recall of CardioFocus Endoscopic Ablation System (EAS) - HeartLight Catheters Lots 7957, 7975, 8006 and 8011, CardioFocus, Inc.
Germany / BfArM · DEU · Apr 10, 2012
Key facts
| Title | Recall of CardioFocus Endoscopic Ablation System (EAS) - HeartLight Catheters Lots 7957, 7975, 8006 and 8011, CardioFocus, Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of CardioFocus Endoscopic Ablation System (EAS) - HeartLight Catheters Lots 7957, 7975, 8006 and 8011, CardioFocus, Inc. |
| Manufacturer | Recall of CardioFocus Endoscopic Ablation System (EAS) - HeartLight Catheters Lots 7957, 7975, 8006 and 8011, CardioFocus, Inc. |
| Models | 500-200, 658-7226, FSCA-2012-001, 01752 |
| Date | Apr 10, 2012 |
| 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