International safety notice
The affected products will be recalled because they were manufactured and shipped during the period when the standard conformity certificate had expired.
Japan / PMDA Recalls · JPN · Aug 1, 2024
Key facts
| Title | The affected products will be recalled because they were manufactured and shipped during the period when the standard conformity certificate had expired. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | General name: Ultrashort wave therapy device Sales name: Physio Radiostim Pro |
| Manufacturer | Ison Co., Ltd. |
| Models | B5J-014, B5J-012, B5J-019, B5J-017, B5J-020, B5J-018, B5J-011, B5J-016, B5J-013, B5J-015 |
| Date | Aug 1, 2024 |
| 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