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 · Sep 17, 2021
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 | 518436, 220308, 516611, 211202, 515653, 516431, 521654, 211007, 513959, 516430, 521857, 72080 and 142 more |
| Event type | Safety Notice |
| Date | Sep 17, 2021 |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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