International safety notice
Urgent Field Safety Notice for OptiSite Arterial Cannula, Femoral Arterial Cannula by Edwards Lifesciences LLC
Germany / BfArM · DEU · Jun 6, 2025
Key facts
| Title | Urgent Field Safety Notice for OptiSite Arterial Cannula, Femoral Arterial Cannula by Edwards Lifesciences LLC |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | OptiSite Arterial Cannula, Femoral Arterial Cannula |
| Manufacturer | Edwards Lifesciences LLC |
| Models | 00690103180558, 95475-252, OPTL16, 00690103031256, FEMII016AS, FEMII018A, 00690103180565, FEMII018AS, FEMII016A, 00690103168341, 00690103031232, 00690103168358 and 2 more |
| Date | Jun 6, 2025 |
| 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