International safety notice
Safety Information and Recall for Penumbra Coil 400, PENUMBRA Inc.
Germany / BfArM · DEU · Apr 1, 2011
Key facts
| Title | Safety Information and Recall for Penumbra Coil 400, PENUMBRA Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Penumbra Coil 400, PENUMBRA Inc. |
| Manufacturer | Safety Information and Recall for Penumbra Coil 400, PENUMBRA Inc. |
| Models | F18184, F18550, 18483, F18520, 17514, F17972, 17448, 17512, 18479, F18121, F17707, F17487 and 148 more |
| Date | Apr 1, 2011 |
| 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