International safety notice
Módulo alicuotador Flexlab, ref de Inpeco FLX-212, ref de Abbott 05P11-19 y 05P66-03
Spain / AEMPS · ESP · Aug 10, 2020
Key facts
| Title | Módulo alicuotador Flexlab, ref de Inpeco FLX-212, ref de Abbott 05P11-19 y 05P66-03 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Módulo alicuotador Flexlab, ref de Inpeco FLX-212, ref de Abbott 05P11-19 y 05P66-03 |
| Manufacturer | Inpeco S.A., Suiza |
| Models | 04S23-07, CHE-114.538.298, 0.ELF, 05P11-19, 9118200, 60064, 91.822.52.89, FLX-212, FA31MAR2020, 2020-466, AQMB_3-1-1-8.H86, 05P66-03MÓDULO and 10 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