International safety notice
Recall of Stent system sinus-Carotid-RX and sinus-Carotid-Conical-RX, optimed GmbH
Germany / BfArM · DEU · Feb 1, 2016
Key facts
| Title | Recall of Stent system sinus-Carotid-RX and sinus-Carotid-Conical-RX, optimed GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of Stent system sinus-Carotid-RX and sinus-Carotid-Conical-RX, optimed GmbH |
| Manufacturer | Recall of Stent system sinus-Carotid-RX and sinus-Carotid-Conical-RX, optimed GmbH |
| Models | 07X20-135, 06X20-135, 6-09X40-135, 06X40-135, 7771-7540, 7769-7540, 07X30-135, 7606-7530, 7771-7530, SIN-CAROT-CRX-5F, 7609-7530, 09X30-135 and 25 more |
| Date | Feb 1, 2016 |
| 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