International safety notice
The manufacturer has reported that this product may cause double image artifacts during use. I understand that. In addition to providing information, we will also conduct product inspections and recall products with confirmed problems.
Japan / PMDA Recalls · JPN · Feb 5, 2024
Key facts
| Title | The manufacturer has reported that this product may cause double image artifacts during use. I understand that. In addition to providing information, we will also conduct product inspections and recall products with confirmed problems. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Ultrasound diagnostic probe for body cavities Sales name: IC9-RS probe |
| Manufacturer | GE Healthcare Japan Co., Ltd. |
| Models | 1083737WX5, 1136324WX9, 1136372WX8, 1136310WX8, 933459WX0, 1089768WX4, 1159016WX3, 1213821WX0, 1143182WX2, 1123072WX9, 1204304WX8, 1087958WX3 and 1062 more |
| Date | Feb 5, 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