International safety notice
Recall for Imager™ II Angiographic catheters and Imager™ II catheters used in urology, Boston Scientific
Germany / BfArM · DEU · Aug 15, 2012
Key facts
| Title | Recall for Imager™ II Angiographic catheters and Imager™ II catheters used in urology, Boston Scientific |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Imager™ II Angiographic catheters and Imager™ II catheters used in urology, Boston Scientific |
| Manufacturer | Recall for Imager™ II Angiographic catheters and Imager™ II catheters used in urology, Boston Scientific |
| Models | 00065399, 00072890, 00068993, 00069467, 31-532, 00064148, 00066622, 00066001, 31-685, 00075214, 00065701, 00067820 and 3258 more |
| Date | Aug 15, 2012 |
| 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