International safety notice
Lot recall of specific EndoWrist® Stapler 45 and 30 instruments for the da Vinci® Xi™ Surgical System, Intuitive Surgical, Inc.
Germany / BfArM · DEU · Aug 31, 2016
Key facts
| Title | Lot recall of specific EndoWrist® Stapler 45 and 30 instruments for the da Vinci® Xi™ Surgical System, Intuitive Surgical, Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the da Vinci® Xi™ Surgical System, Intuitive Surgical, Inc. |
| Manufacturer | Lot recall of specific EndoWrist® Stapler 45 and 30 instruments for the da Vinci® Xi™ Surgical System, Intuitive Surgical, Inc. |
| Models | 16-010-R, 470530, 876-1310, 2955842-07, CH-1170, 03-5575-1362, 470298, 0120-56-5635, 523-0619, 02-3271-3200, 470430, 800-876-1310 |
| Date | Aug 31, 2016 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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