International safety notice
Alinity m HCV AMP Kit, número de referencia: 08N50-090. Ver UDI en la nota de aviso de la empresa.
Spain / AEMPS · ESP · Nov 14, 2023
Key facts
| Title | Alinity m HCV AMP Kit, número de referencia: 08N50-090. Ver UDI en la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Alinity m HCV AMP Kit, número de referencia: 08N50-090. Ver UDI en la nota de aviso de la empresa. |
| Manufacturer | Abbott Molecular, Inc., EE.UU. |
| Models | 09N33-020, 1.8.0, 08N50-090, 382447, 2022-12-16, 381581, 28022, 99415, G9-5428R14, 383203, 385720, 2023-521 and 6 more |
| Event type | Safety Notice |
| Date | Nov 14, 2023 |
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