International safety notice
Kit Alinity m Resp-4-Plex AMP, referencia: 09N79-090. Ver los UDI afectados en la nota de aviso de la empresa.
Spain / AEMPS · ESP · May 26, 2025
Key facts
| Title | Kit Alinity m Resp-4-Plex AMP, referencia: 09N79-090. Ver los UDI afectados en la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Kit Alinity m Resp-4-Plex AMP, referencia: 09N79-090. Ver los UDI afectados en la nota de aviso de la empresa. |
| Manufacturer | Abbott Molecular, Inc., EEUU. |
| Models | RESP-4-PLEX, 09N79-090 |
| Event type | Safety Notice |
| Date | May 26, 2025 |
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