International safety notice
General name: Anti-acting vagus nerve electrical stimulation device Sales name: Vagal nerve stimulation device SenTiva
Japan / PMDA Recalls · JPN · Jan 27, 2025
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | General name: Anti-acting vagus nerve electrical stimulation device Sales name: Vagal nerve stimulation device SenTiva |
| Manufacturer | Rivanova Inc. |
| Models | 367249, 350915, 344547, 332443, 320103, 329360, 342153, 368882, 341523, 323820, 329914, 327576 and 911 more |
| Date | Jan 27, 2025 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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