International safety notice
Recall of the CoStar® Paclitaxel-Eluting Coronary Stent Systems from CONOR Medsystems
Germany / BfArM · DEU · Jun 25, 2007
Key facts
| Title | Recall of the CoStar® Paclitaxel-Eluting Coronary Stent Systems from CONOR Medsystems |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the CoStar® Paclitaxel-Eluting Coronary Stent Systems from CONOR Medsystems |
| Manufacturer | Recall of the CoStar® Paclitaxel-Eluting Coronary Stent Systems from CONOR Medsystems |
| Models | 43533810, 359380, 359382, 6F4.412S, 427528810, 359378, CAS402S, 351541, 43022810, 351536, 351533, 42753330 and 35 more |
| Date | Jun 25, 2007 |
| 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