International safety notice
Angiomed recalls Bard® LUMINEXX® Endoscopic Biliary Stent and Bard® memotherm® Colorectal Stent
Germany / BfArM · DEU · Sep 9, 2005
Key facts
| Title | Angiomed recalls Bard® LUMINEXX® Endoscopic Biliary Stent and Bard® memotherm® Colorectal Stent |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Angiomed recalls Bard® LUMINEXX® Endoscopic Biliary Stent and Bard® memotherm® Colorectal Stent |
| Manufacturer | Angiomed recalls Bard® LUMINEXX® Endoscopic Biliary Stent and Bard® memotherm® Colorectal Stent |
| Models | 79936, 12055, 1.800-448-6506 |
| Date | Sep 9, 2005 |
| 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