International safety notice
Dispositivos de anestesia Aisys mejorados con las versiones de software 11SP01 o 11SP02 y Dispositivos de anestesia Aisys CS2 con las versiones de software 11SP01 o 11SP02 y la opción End Tidal Control (Et Control).
Spain / AEMPS · ESP · Apr 15, 2019
Key facts
| Title | Dispositivos de anestesia Aisys mejorados con las versiones de software 11SP01 o 11SP02 y Dispositivos de anestesia Aisys CS2 con las versiones de software 11SP01 o 11SP02 y la opción End Tidal Control (Et Control). |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Dispositivos de anestesia Aisys mejorados con las versiones de software 11SP01 o 11SP02 y Dispositivos de anestesia Aisys CS2 con las versiones de software 11SP01 o 11SP02 y la opción End Tidal Control (Et Control). |
| Manufacturer | Datex-Ohmeda, Inc., EEUU. |
| Models | 35-37, 28023, 51468, 11SP02, 53188, 902118226, 11SP01, SOFTWARE11SP01, 34094, 840682102292, 28022, 34098 and 2 more |
| Event type | Safety Notice |
| Date | Apr 15, 2019 |
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