International safety notice
Angiomed recalls Bard® LUMINEXX® 3 Biliary and Vascular Stents and Bard® LUMINEXX® 6 F Vascular Stents
Germany / BfArM · DEU · Aug 11, 2005
Key facts
| Title | Angiomed recalls Bard® LUMINEXX® 3 Biliary and Vascular Stents and Bard® LUMINEXX® 6 F Vascular Stents |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Angiomed recalls Bard® LUMINEXX® 3 Biliary and Vascular Stents and Bard® LUMINEXX® 6 F Vascular Stents |
| Manufacturer | Angiomed recalls Bard® LUMINEXX® 3 Biliary and Vascular Stents and Bard® LUMINEXX® 6 F Vascular Stents |
| Models | 49-721-9445-142 |
| Date | Aug 11, 2005 |
| 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