International safety notice
Analizador de inmunoensayo DxI 9000 Access, referencia C11137.
Spain / AEMPS · ESP · Mar 15, 2024
Key facts
| Title | Analizador de inmunoensayo DxI 9000 Access, referencia C11137. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Analizador de inmunoensayo DxI 9000 Access, referencia C11137. |
| Manufacturer | Beckman Coulter, EEUU. |
| Models | 300272, 91.822.52.89, 300257, 2024-136, 300258, 300266, 41-43, 300259, 300268, 104028, 300275, 300282 and 13 more |
| Event type | Safety Notice |
| Date | Mar 15, 2024 |
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