International safety notice
General name: Reusable hand-controlled electrosurgical instrument active electrode Sales name: AARON900 Electrosurgical instrument components foot switch
Japan / PMDA Recalls · JPN · Jun 30, 2025
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | General name: Reusable hand-controlled electrosurgical instrument active electrode Sales name: AARON900 Electrosurgical instrument components foot switch |
| Manufacturer | Gunze Medical Co., Ltd. |
| Models | 409951 |
| Date | Jun 30, 2025 |
| 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