International safety notice
Common name: Multi-item monitor with important parameters Brand name: Carescape Patient Data Module
Japan / PMDA Recalls · JPN · Jun 25, 2021
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | Common name: Multi-item monitor with important parameters Brand name: Carescape Patient Data Module |
| Manufacturer | GE Healthcare Japan Co., Ltd. |
| Models | SA317070202SA, SA315229807GA, SPX18460449SA, SA310058729GA, SPX17470239SA, SA317160074SA, SA317160069SA, SA317160104SA, SPX20190529SA, SPX18460448SA, SPX17470250SA, SA309193271GA and 282 more |
| Date | Jun 25, 2021 |
| 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