International safety notice
Recall for Neuron 070 Delivery Catheter, Penumbra Inc.
Germany / BfArM · DEU · Oct 13, 2009
Key facts
| Title | Recall for Neuron 070 Delivery Catheter, Penumbra Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Neuron 070 Delivery Catheter, Penumbra Inc. |
| Manufacturer | Recall for Neuron 070 Delivery Catheter, Penumbra Inc. |
| Models | 676-0, F13799, F13733, F13899, F14028, 510-748—, F14560, PND6F0701058M, F14629, F14482, 510-217—, F14007 and 30 more |
| Date | Oct 13, 2009 |
| 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