International safety notice
Recall of Expo™ und Impulse™ Angiographic Catheters from Boston Scientific
Germany / BfArM · DEU · Jul 24, 2006
Key facts
| Title | Recall of Expo™ und Impulse™ Angiographic Catheters from Boston Scientific |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of Expo™ und Impulse™ Angiographic Catheters from Boston Scientific |
| Manufacturer | Recall of Expo™ und Impulse™ Angiographic Catheters from Boston Scientific |
| Models | NFPB-2, 1474916391, 74916391, 2006-26, MPA-2, H749085261212, 08526-121, 571479, 16391-122, FCA2006-26, 1-174916391, 1-174908526121 and 12 more |
| Date | Jul 24, 2006 |
| 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