International safety notice
Urgent Field Safety Notice for Atellica IM Erythropoietin (EPO) Assay; ADVIA Centaur Erythropoietin (EPO) Assay; by Siemens Healthcare Diagnostics Inc. Tarrytown
Germany / BfArM · DEU · Feb 29, 2024
Key facts
| Title | Urgent Field Safety Notice for Atellica IM Erythropoietin (EPO) Assay; ADVIA Centaur Erythropoietin (EPO) Assay; by Siemens Healthcare Diagnostics Inc. Tarrytown |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Atellica IM Erythropoietin (EPO) Assay; ADVIA Centaur Erythropoietin (EPO) Assay; |
| Manufacturer | Siemens Healthcare Diagnostics Inc. Tarrytown |
| Models | 2023-02-09, 00630414010380, 2024-02-05, 53984040, 55439041, 53982039, 55443042, 20240820, 20240205, 00630414245775, 20230209, 2023-02-08 and 7 more |
| Date | Feb 29, 2024 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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