International safety notice
ORTHO® T. cruzi ELISA Test System. Ver códigos de productos y UDI afectados en la nota de aviso de la empresa
Spain / AEMPS · ESP · Dec 28, 2021
Key facts
| Title | ORTHO® T. cruzi ELISA Test System. Ver códigos de productos y UDI afectados en la nota de aviso de la empresa |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | ORTHO® T. cruzi ELISA Test System. Ver códigos de productos y UDI afectados en la nota de aviso de la empresa |
| Manufacturer | Ortho Clinical Diagnostics Inc., Estados Unidos |
| Models | 6195567, 10758750005260, E631202442, E631209801, 10758750007479, E631209809, 75179, E631201615, J68332, 2021-713, 2021PUEDE, E631201328 and 30 more |
| Event type | Safety Notice |
| Date | Dec 28, 2021 |
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