International safety notice
Recall for Renegade Fiber Braided Microcatheter, Renegade Hi-Flo Microcatheter and Renegade Hi-Flo Microcatheter Kits, Boston Scientific
Germany / BfArM · DEU · Sep 14, 2009
Key facts
| Title | Recall for Renegade Fiber Braided Microcatheter, Renegade Hi-Flo Microcatheter and Renegade Hi-Flo Microcatheter Kits, Boston Scientific |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Renegade Fiber Braided Microcatheter, Renegade Hi-Flo Microcatheter and Renegade Hi-Flo Microcatheter Kits, Boston Scientific |
| Manufacturer | Recall for Renegade Fiber Braided Microcatheter, Renegade Hi-Flo Microcatheter and Renegade Hi-Flo Microcatheter Kits, Boston Scientific |
| Models | 11432586, 12509937, 12091511, 11294909, 12541271, 12578823, 12402114, 11512538, 12365631, 12703134, 11934442, 12-FA and 2654 more |
| Date | Sep 14, 2009 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers 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