International safety notice
Ensayo de Estradiol E2 para los sistemas IMMULITE. Ver nos de referencia y lotes afectados en la nota de aviso de la empresa.
Spain / AEMPS · ESP · Feb 24, 2020
Key facts
| Title | Ensayo de Estradiol E2 para los sistemas IMMULITE. Ver nos de referencia y lotes afectados en la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Ensayo de Estradiol E2 para los sistemas IMMULITE. Ver nos de referencia y lotes afectados en la nota de aviso de la empresa. |
| Manufacturer | Siemens Healthcare Diagnostics Products Limited, Reino Unido. |
| Models | 10381132, 10591, 10381177, 901116359, 28022, LKE21, 28906, L2KE26, ESTRADIOL-17B, 58082, IMC20-01.A.OUS, 10381178 and 3 more |
| Event type | Safety Notice |
| Date | Feb 24, 2020 |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 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