International safety notice
General names: (1)-(2) Reusable active endoscopic instruments for high-frequency treatments, (3) Reusable active endoscopic treatments Sales name: (1)HF-II series bipoline strument (2)HF-II Series Monopole Line Strument (3)HF-II Series Instruments
Japan / PMDA Recalls · JPN · Apr 18, 2025
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | General names: (1)-(2) Reusable active endoscopic instruments for high-frequency treatments, (3) Reusable active endoscopic treatments Sales name: (1)HF-II series bipoline strument (2)HF-II Series Monopole Line Strument (3)HF-II Series Instruments |
| Manufacturer | Medicaroid Co., Ltd. |
| Models | 100217011, 100355011, 100200011, 100066011, 100049011, 100524011, 100289011, 100570011, 100352011, 100183011, 100572011, 100512011 and 578 more |
| Date | Apr 18, 2025 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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