International safety notice
Kit Alinity m Resp-4-Plex AMP, referencia: 09N79-090.
Spain / AEMPS · ESP · Dec 14, 2022
Key facts
| Title | Kit Alinity m Resp-4-Plex AMP, referencia: 09N79-090. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Kit Alinity m Resp-4-Plex AMP, referencia: 09N79-090. |
| Manufacturer | Abbott Molecular, Inc., EEUU. |
| Models | 527602, 525766, 230115, 230208, 230129, 28022, 531612, 91.822.52.89, 526483, 2022-540, 230121, 09N79-090 and 15 more |
| Event type | Safety Notice |
| Date | Dec 14, 2022 |
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