International safety notice
Recall for SoloPath™ Balloon Expandable Transfemoral Introducer, Onset Medical Corporation
Germany / BfArM · DEU · Dec 14, 2010
Key facts
| Title | Recall for SoloPath™ Balloon Expandable Transfemoral Introducer, Onset Medical Corporation |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | SoloPath™ Balloon Expandable Transfemoral Introducer, Onset Medical Corporation |
| Manufacturer | Recall for SoloPath™ Balloon Expandable Transfemoral Introducer, Onset Medical Corporation |
| Models | 13900, 92618, 949.716.1100, 949.716.1101 |
| Date | Dec 14, 2010 |
| 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