International safety notice
Recall of NexStent™ Monorail™ Carotid Stent systems, Boston Scientific
Germany / BfArM · DEU · May 30, 2006
Key facts
| Title | Recall of NexStent™ Monorail™ Carotid Stent systems, Boston Scientific |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of NexStent™ Monorail™ Carotid Stent systems, Boston Scientific |
| Manufacturer | Recall of NexStent™ Monorail™ Carotid Stent systems, Boston Scientific |
| Models | 51301, 51403, C52202, 51602, 50401, C50502, 50406, 50302, 51803, 51701, 52203, C50303 and 154 more |
| Date | May 30, 2006 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 1,000+ 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