International safety notice
Prismax, V2 ROW, código de producto: 955558; Prismax, V3 unidad de control ROW, código de producto: 955725
Spain / AEMPS · ESP · Mar 30, 2022
Key facts
| Title | Prismax, V2 ROW, código de producto: 955558 ; Prismax, V3 unidad de control ROW, código de producto: 955725 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Prismax, V2 ROW, código de producto: 955558 ; Prismax, V3 unidad de control ROW, código de producto: 955725 |
| Manufacturer | Baxter Healthcare SA, Suiza |
| Models | 955558PRISMAX, 955725, 78377, 955558, 46394, 28022, FA-2022-006, 2022-153, 91.822.52.89, 962.722.894 |
| Event type | Safety Notice |
| Date | Mar 30, 2022 |
At a glance
- No Recall
- Yes 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