International safety notice
Through an investigation by our manufacturer, we have confirmed an issue in the manufacturing process of the grip at the tip (the part that grips tissue). Ta. We have decided to do so.
Japan / PMDA Recalls · JPN · Jun 7, 2023
Key facts
| Title | Through an investigation by our manufacturer, we have confirmed an issue in the manufacturing process of the grip at the tip (the part that grips tissue). Ta. We have decided to do so. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Reusable endoscopic active treatment device Sales name: EndoWrist Instrument |
| Manufacturer | Intuitive Surgical LLC |
| Models | 470347-12 |
| Date | Jun 7, 2023 |
| Regulator page | info.pmda.go.jp |
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