International safety notice
Recall for Visi-Pro Balloon Expandable Stent System, ev3 Inc.
Germany / BfArM · DEU · Jul 25, 2008
Key facts
| Title | Recall for Visi-Pro Balloon Expandable Stent System, ev3 Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Visi-Pro Balloon Expandable Stent System, ev3 Inc. |
| Manufacturer | Recall for Visi-Pro Balloon Expandable Stent System, ev3 Inc. |
| Models | 33-156, 33-686 |
| Date | Jul 25, 2008 |
| 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