International safety notice
Corrective action for the da Vinci Si EndoWrist® One Vessel Sealer and da Vinci Xi EndoWrist® Vessel Sealer, Intuitive Surgical Sàrl
Germany / BfArM · DEU · Mar 11, 2015
Key facts
| Title | Corrective action for the da Vinci Si EndoWrist® One Vessel Sealer and da Vinci Xi EndoWrist® Vessel Sealer, Intuitive Surgical Sàrl |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the da Vinci Si EndoWrist® One Vessel Sealer and da Vinci Xi EndoWrist® Vessel Sealer, Intuitive Surgical Sàrl |
| Manufacturer | Corrective action for the da Vinci Si EndoWrist® One Vessel Sealer and da Vinci Xi EndoWrist® Vessel Sealer, Intuitive Surgical Sàrl |
| Models | S10140916, M10140818, M11140828, M11140818, S10141125, M10141201, S10140923, M10140828, M11140917, S10141001, M10141022, S10141020 and 67 more |
| Date | Mar 11, 2015 |
| 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