International safety notice
Reactivos Atellica IM CA 19-9 y Advia Centaur CA 19-9. Ver número de material de Siemens y UDI en la nota de aviso de la empresa.
Spain / AEMPS · ESP · Aug 8, 2024
Key facts
| Title | Reactivos Atellica IM CA 19-9 y Advia Centaur CA 19-9. Ver número de material de Siemens y UDI en la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Reactivos Atellica IM CA 19-9 y Advia Centaur CA 19-9. Ver número de material de Siemens y UDI en la nota de aviso de la empresa. |
| Manufacturer | Siemens Healthcare Diagnostics Inc., EEUU. |
| Models | US-MF-000016560, 55971535, 00630414574257, 14-NOV-2023, 28043, 10491379, 55973535, 98178, 10995490, 19-9.VER, 91.822.52.89, 2024-436 and 15 more |
| Event type | Safety Notice |
| Date | Aug 8, 2024 |
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