International safety notice
Recall of Guider Guide Catheter, Stryker Neurovascular
Germany / BfArM · DEU · Oct 17, 2016
Key facts
| Title | Recall of Guider Guide Catheter, Stryker Neurovascular |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of Guider Guide Catheter, Stryker Neurovascular |
| Manufacturer | Recall of Guider Guide Catheter, Stryker Neurovascular |
| Models | 18771332, 18753510, 18774858, 18790229, 18848795, 18903165, 18829078, 18786441, M003101640, 18904600, 18714267, 18726453 and 56 more |
| Date | Oct 17, 2016 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models 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