International safety notice
Recall of IntrepideTM coronary stent system, ClearStream
Germany / BfArM · DEU · Sep 30, 2010
Key facts
| Title | Recall of IntrepideTM coronary stent system, ClearStream |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of IntrepideTM coronary stent system, ClearStream |
| Manufacturer | Recall of IntrepideTM coronary stent system, ClearStream |
| Models | 39240016, 39240024, 39235024, 37111-215, 39240012, 39225028, 39225024, 39227520, 39230024, FSN002, 39230016, 39235016 and 28 more |
| Date | Sep 30, 2010 |
| 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