International safety notice
Recall for BigLumen Aspiration catheter, OptiMed
Germany / BfArM · DEU · Sep 11, 2008
Key facts
| Title | Recall for BigLumen Aspiration catheter, OptiMed |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | BigLumen Aspiration catheter, OptiMed |
| Manufacturer | Recall for BigLumen Aspiration catheter, OptiMed |
| Models | 76275, 6000015766, 1720-2070 |
| Date | Sep 11, 2008 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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