International safety notice
Recall of the product LeGoo Endovascular Occlusion Gel, Genzyme Corporation (Sanofi)
Germany / BfArM · DEU · Nov 19, 2013
Key facts
| Title | Recall of the product LeGoo Endovascular Occlusion Gel, Genzyme Corporation (Sanofi) |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the product LeGoo Endovascular Occlusion Gel, Genzyme Corporation (Sanofi) |
| Manufacturer | Recall of the product LeGoo Endovascular Occlusion Gel, Genzyme Corporation (Sanofi) |
| Models | 10-0250, LG50IT, 10-0100, 781-932-0574, CR01450, LG250IT, 10-0025, 10-0500, 01801, 10-1000, 11-27, LG100IT and 1 more |
| Date | Nov 19, 2013 |
| 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