International safety notice
Recall for the RotaWire Elite™ Guidewire and wireClip™ Torquer Guidewire Manipulation Device, Boston Scientific International S.A.
Germany / BfArM · DEU · Oct 19, 2015
Key facts
| Title | Recall for the RotaWire Elite™ Guidewire and wireClip™ Torquer Guidewire Manipulation Device, Boston Scientific International S.A. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the RotaWire Elite™ Guidewire and wireClip™ Torquer Guidewire Manipulation Device, Boston Scientific International S.A. |
| Manufacturer | Recall for the RotaWire Elite™ Guidewire and wireClip™ Torquer Guidewire Manipulation Device, Boston Scientific International S.A. |
| Models | 18362094, 18378161, H802233300, 18201519, 18390089, 95941, H802233301, 93420, 18141187, 18194620, 5-PACKS, 00035 and 17 more |
| Date | Oct 19, 2015 |
| 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