International safety notice
Lot Recall for Reperfusion Catheter 032, Penumbra
Germany / BfArM · DEU · Dec 8, 2010
Key facts
| Title | Lot Recall for Reperfusion Catheter 032, Penumbra |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Reperfusion Catheter 032, Penumbra |
| Manufacturer | Lot Recall for Reperfusion Catheter 032, Penumbra |
| Models | 94502, F15020, 15-NOVEMBER-2010, 510-748•—, 11-10, PSC032, 49-30-200, 15020 |
| Date | Dec 8, 2010 |
| 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