International safety notice
VITROS 3600 Immunodiagnostic Systems y VITROS 5600/XT 7600 Integrated Systems. Ver códigos y UDIs de los productos afectados en la nota de aviso de la empresa.
Spain / AEMPS · ESP · Jan 30, 2024
Key facts
| Title | VITROS 3600 Immunodiagnostic Systems y VITROS 5600/XT 7600 Integrated Systems. Ver códigos y UDIs de los productos afectados en la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | VITROS 3600 Immunodiagnostic Systems y VITROS 5600/XT 7600 Integrated Systems. Ver códigos y UDIs de los productos afectados en la nota de aviso de la empresa. |
| Manufacturer | QuidelOrtho (Ortho Clinical Diagnostics Inc)., EEUU. |
| Models | 28033, J56001998, J36001692, J56000330, J56000721, J56001834, J56001855, J56001228, J56001355, J56002655, J56000839, J56003170 and 40 more |
| Event type | Safety Notice |
| Date | Jan 30, 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