International safety notice
Recall of VI AUF Stent Graft and VI Extender Cuff from INTERVASCULAR
Germany / BfArM · DEU · Nov 16, 2006
Key facts
| Title | Recall of VI AUF Stent Graft and VI Extender Cuff from INTERVASCULAR |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of VI AUF Stent Graft and VI Extender Cuff from INTERVASCULAR |
| Manufacturer | Recall of VI AUF Stent Graft and VI Extender Cuff from INTERVASCULAR |
| Models | 13705, 101050106, AUF-SG-0125, 102170206, V101240106, V101090206, V102080206, 190406, 00012, AUF-EC-0225, V102230106, NAF702 and 5 more |
| Date | Nov 16, 2006 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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