International safety notice
Módulo alicuotador (AQM) incluido en el sistema Accelerator a3600, número de referencia de Inpeco FLX-212, número de referencia de Abbott 06P47, versiones de firmware: AQMb_3-3-0.H86, AQMa_3-1-1-8.H86 y AQMb_3-1-1-8.H86 o posteriores.
Spain / AEMPS · ESP · Aug 10, 2020
Key facts
| Title | Módulo alicuotador (AQM) incluido en el sistema Accelerator a3600, número de referencia de Inpeco FLX-212, número de referencia de Abbott 06P47, versiones de firmware: AQMb_3-3-0.H86, AQMa_3-1-1-8.H86 y AQMb_3-1-1-8.H86 o posteriores. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Módulo alicuotador (AQM) incluido en el sistema Accelerator a3600, número de referencia de Inpeco FLX-212, número de referencia de Abbott 06P47, versiones de firmware: AQMb_3-3-0.H86, AQMa_3-1-1-8.H86 y AQMb_3-1-1-8.H86 o posteriores. |
| Manufacturer | Inpeco S.A., Suiza |
| Models | 2020-465, AQMB_3-3-0.H86, 60064, 28050, 202003, 61260, 02_A3600_OUS, 28022, AQMB_3-1-1-8.H86, CHE-114.538.298, 9118200, FA31MAR2020 and 6 more |
| Event type | Safety Notice |
| Date | Aug 10, 2020 |
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