International safety notice
Urgent Safety Notice on PTA Balloon Dilatation Catheter product families (Models Coyote™ Over-The-Wire and Coyote™ Monorail™), Boston Scientific International
Germany / BfArM · DEU · Feb 14, 2014
Key facts
| Title | Urgent Safety Notice on PTA Balloon Dilatation Catheter product families (Models Coyote™ Over-The-Wire and Coyote™ Monorail™), Boston Scientific International |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Urgent Safety Notice on PTA Balloon Dilatation Catheter product families (Models Coyote™ Over-The-Wire and Coyote™ Monorail™), Boston Scientific International |
| Manufacturer | Urgent Safety Notice on PTA Balloon Dilatation Catheter product families (Models Coyote™ Over-The-Wire and Coyote™ Monorail™), Boston Scientific International |
| Models | H74939186251210, 16397693, 39185-20151, 39186-25121, 90917431-FA, 16310947, H74939185201510 |
| Date | Feb 14, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 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