International safety notice
Recall of specific lots of the Large Needle Driver and Mega Needle Driver EndoWrist® Instruments for da Vinci® Surgical Systems, Intuitive Surgical
Germany / BfArM · DEU · Dec 9, 2013
Key facts
| Title | Recall of specific lots of the Large Needle Driver and Mega Needle Driver EndoWrist® Instruments for da Vinci® Surgical Systems, Intuitive Surgical |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | da Vinci® Surgical Systems, Intuitive Surgical |
| Manufacturer | Recall of specific lots of the Large Needle Driver and Mega Needle Driver EndoWrist® Instruments for da Vinci® Surgical Systems, Intuitive Surgical |
| Models | 711052, M10100203, M10091022, M10101214, 801092, M10110728, M10080902, M10101112, M10110714, M10090916, 805051, M10110523 and 831 more |
| Date | Dec 9, 2013 |
| 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