International safety notice
Analizadores Atellica IM 1300 y 1600, cuando utilizan determinados recipientes para muestras Atellica.
Spain / AEMPS · ESP · May 25, 2020
Key facts
| Title | Analizadores Atellica IM 1300 y 1600, cuando utilizan determinados recipientes para muestras Atellica. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Analizadores Atellica IM 1300 y 1600, cuando utilizan determinados recipientes para muestras Atellica. |
| Manufacturer | Siemens Healthcare Diagnostics Products GmbH, Alemania |
| Models | 91.822.52.89, 11069101, 11066001, 2020-267, 59089, 901116359, 11069061, 28022, 11066000, 62.612, 11069062, ASI20-02.A.OUS and 1 more |
| Event type | Safety Notice |
| Date | May 25, 2020 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 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