International safety notice
Urgent Field Safety Notice for Pipeline Flex Embolization Device by Micro Therapeutics, Inc. DBA ev3 Neurovascular
Germany / BfArM · DEU · Aug 3, 2021
Key facts
| Title | Urgent Field Safety Notice for Pipeline Flex Embolization Device by Micro Therapeutics, Inc. DBA ev3 Neurovascular |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Pipeline Flex Embolization Device |
| Manufacturer | Micro Therapeutics, Inc. DBA ev3 Neurovascular |
| Models | A867839, B007408, B018629, A909370, A876746, A879718, A858334, A818295, A816345, A821014, A833121, B007368 and 1815 more |
| Date | Aug 3, 2021 |
| 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