International safety notice
Recall for the Endoplege Coronary Sinus Catheter Kit, Edwards Lifesciences
Germany / BfArM · DEU · Sep 22, 2011
Key facts
| Title | Recall for the Endoplege Coronary Sinus Catheter Kit, Edwards Lifesciences |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Endoplege Coronary Sinus Catheter Kit, Edwards Lifesciences |
| Manufacturer | Recall for the Endoplege Coronary Sinus Catheter Kit, Edwards Lifesciences |
| Models | 774336B, 774337, 763119B, 848628, 856502, 794302B, 856509, 763125B, «ADD_2», 821595, 798587, 841434 and 26 more |
| Date | Sep 22, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No 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