International safety notice
Reactivo Access Eritropoyetina (EPO), referencia A16364. UDI: 15099590201838
Spain / AEMPS · ESP · Feb 19, 2025
Key facts
| Title | Reactivo Access Eritropoyetina (EPO), referencia A16364. UDI: 15099590201838 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Reactivo Access Eritropoyetina (EPO), referencia A16364. UDI: 15099590201838 |
| Manufacturer | Beckman Coulter, Inc., EEUU. |
| Models | 15099590201838, A16364 |
| Event type | Safety Notice |
| Date | Feb 19, 2025 |
At a glance
- No Recall
- Yes 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