International safety notice
Recall of the Carotid Wallstent™ Endoprosthesis with Monorail™ Delivery System from Boston Scientific
Germany / BfArM · DEU · Apr 2, 2007
Key facts
| Title | Recall of the Carotid Wallstent™ Endoprosthesis with Monorail™ Delivery System from Boston Scientific |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the Carotid Wallstent™ Endoprosthesis with Monorail™ Delivery System from Boston Scientific |
| Manufacturer | Recall of the Carotid Wallstent™ Endoprosthesis with Monorail™ Delivery System from Boston Scientific |
| Models | 0009138720, 0009162504, 0009370662, SCH647-13, 0009156004, 03-MAY-2010, 0009158989, 0009122441, 0009157032, 01-APR-2010, 0009155744, 0009098967 and 149 more |
| Date | Apr 2, 2007 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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