International safety notice
Kit de reactivos Alinity i HBsAg, número de referencia: 07P8952 y UDI (01)00380740138219(17)240630
Spain / AEMPS · ESP · Feb 2, 2024
Key facts
| Title | Kit de reactivos Alinity i HBsAg, número de referencia: 07P8952 y UDI (01)00380740138219(17)240630 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Kit de reactivos Alinity i HBsAg, número de referencia: 07P8952 y UDI (01)00380740138219(17)240630 |
| Manufacturer | Abbott Ireland Diagnostics Division, Irlanda |
| Models | 28022, LOTE51441FN00, 102227, 2024-064, 07P8952, 51441FN00, 00380740138219, 91.822.52.89, 51503FN00, IE-MF-000009849, 240630 |
| Event type | Safety Notice |
| Date | Feb 2, 2024 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models 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