International safety notice
PrisMax, V2, Row, referencia 955558.
Spain / AEMPS · ESP · Aug 22, 2019
Key facts
| Title | PrisMax, V2, Row, referencia 955558. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | PrisMax, V2, Row, referencia 955558. |
| Manufacturer | Baxter Healthcare, SA, Suiza. |
| Models | 100516, 100853, 2019PUEDE, 100676, 96.272.28.00, 100409, 955558, T0850, 46394, 91.822.52.89, 100673, T0525 and 15 more |
| Event type | Safety Notice |
| Date | Aug 22, 2019 |
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