International safety notice
Common name: Multi-item monitor with important parameters Sales name: Hemosphere Advanced Monitoring Platform
Japan / PMDA Recalls · JPN · Mar 10, 2023
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | Common name: Multi-item monitor with important parameters Sales name: Hemosphere Advanced Monitoring Platform |
| Manufacturer | Edwards Lifesciences Co., Ltd. |
| Models | 21104849, 21101167, 21101384, 21104851, 21101134, 21106753, 21101447, 21120224, 21102636, 21106911, 21102818, 21106453 and 585 more |
| Date | Mar 10, 2023 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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