International safety notice
Reactivo cobas® SARS-CoV-2 & Influenza A/B Test (referencia: 09211101190; identificador: 00875197006360) para uso en cobas® Liat® System (referencia: 07341920190; identificador: 07613336100097).
Spain / AEMPS · ESP · Mar 26, 2021
Key facts
| Title | Reactivo cobas® SARS-CoV-2 & Influenza A/B Test (referencia: 09211101190; identificador: 00875197006360) para uso en cobas® Liat® System (referencia: 07341920190; identificador: 07613336100097). |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Reactivo cobas® SARS-CoV-2 & Influenza A/B Test (referencia: 09211101190; identificador: 00875197006360) para uso en cobas® Liat® System (referencia: 07341920190; identificador: 07613336100097). |
| Manufacturer | Roche Molecular Systems, Estados Unidos. |
| Models | 2021PUEDE, 2021-168, 00875197006360, 09211101190, SARS-COV-2, COVID-19, 07341920190, 91.822.52.89, 171-173, V3.3.0, 28022, MAR-2021 and 12 more |
| Event type | Safety Notice |
| Date | Mar 26, 2021 |
At a glance
- No Recall
- Yes Field safety notice
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