International safety notice
Stryker Neurovascular: Recall for Excelsior Microcatheters, GDC Coils, Neuroform EZ Stents and Transform Balloons
Germany / BfArM · DEU · Jan 21, 2014
Key facts
| Title | Stryker Neurovascular: Recall for Excelsior Microcatheters, GDC Coils, Neuroform EZ Stents and Transform Balloons |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Excelsior Microcatheters, GDC Coils, Neuroform EZ Stents and Transform Balloons |
| Manufacturer | Stryker Neurovascular: Recall for Excelsior Microcatheters, GDC Coils, Neuroform EZ Stents and Transform Balloons |
| Models | M003SSC04070, 17010924, 17010880, 17027074, M003EN3E35150, 17020619, 17048727, 17010749, M0033432030, 17046274, 17026849, M003EN3E40150 and 77 more |
| Date | Jan 21, 2014 |
| 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