International safety notice
• Alinity m SARS-CoV-2 AMP Kit, números de referencia 09N78-090 o 09N78-091, • Alinity m Resp-4-Plex AMP Kit, número de referencia 09N79-090
Spain / AEMPS · ESP · Apr 12, 2022
Key facts
| Title | • Alinity m SARS-CoV-2 AMP Kit, números de referencia 09N78-090 o 09N78-091, • Alinity m Resp-4-Plex AMP Kit, número de referencia 09N79-090 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | • Alinity m SARS-CoV-2 AMP Kit, números de referencia 09N78-090 o 09N78-091, • Alinity m Resp-4-Plex AMP Kit, número de referencia 09N79-090 |
| Manufacturer | Abbott Molecular, Inc., EEUU. |
| Models | 09N78-01E, FA-AM-SEP2021-260BV2, 00884999049338, 72080, 91.822.52.89, 00884999050228, RESP-4-PLEX, 09N78-090, 09N79-01D, 0.0016, 09N78-091, SARSCOV-2 and 15 more |
| Event type | Safety Notice |
| Date | Apr 12, 2022 |
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