International safety notice
Recall for Wiseguide™ Guide Catheters, Impulse™ and Expo™ Angiographic Catheters, Boston Scientific
Germany / BfArM · DEU · Aug 20, 2009
Key facts
| Title | Recall for Wiseguide™ Guide Catheters, Impulse™ and Expo™ Angiographic Catheters, Boston Scientific |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Wiseguide™ Guide Catheters, Impulse™ and Expo™ Angiographic Catheters, Boston Scientific |
| Manufacturer | Recall for Wiseguide™ Guide Catheters, Impulse™ and Expo™ Angiographic Catheters, Boston Scientific |
| Models | 5-PACKS, 90519291-FA, 1.3-AUG-2ZZB, «CUSTOMER_SERVICE_TE1» |
| Date | Aug 20, 2009 |
| 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