International safety notice
OptiMed recalls its "sinus-Carotid-RX-Systems". It was reported that the stent was difficult or not able to be released.
Germany / BfArM · DEU · Sep 8, 2006
Key facts
| Title | OptiMed recalls its "sinus-Carotid-RX-Systems". It was reported that the stent was difficult or not able to be released. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | OptiMed recalls its "sinus-Carotid-RX-Systems". It was reported that the stent was difficult or not able to be released. |
| Manufacturer | OptiMed recalls its "sinus-Carotid-RX-Systems". It was reported that the stent was difficult or not able to be released. |
| Models | CAROTID—CONICA1—RX, 76275 |
| Date | Sep 8, 2006 |
| 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