International safety notice
Módulo alicuotador incluido en los sistemas de automatización Flexlab, SMN 10628151 y Flexlab HS, SMN 10720943, 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 14, 2020
Key facts
| Title | Módulo alicuotador incluido en los sistemas de automatización Flexlab, SMN 10628151 y Flexlab HS, SMN 10720943, 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 incluido en los sistemas de automatización Flexlab, SMN 10628151 y Flexlab HS, SMN 10720943, 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 | 10628151, FLX-212, AQMA_3-1-1-8.H86, 61259, MOD-FSN.02, 28906, 91.822.52.89, 10720943, CHE-114.538.298, 8.H86, 2020-475, AQMB_3-1-1-8.H86 and 9 more |
| Event type | Safety Notice |
| Date | Aug 14, 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