Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 23742 |
| Brand Name: | Anaesthesia Work Stations |
| Model: | All upgraded Aisys anesthesia devices (i.e. Aisys devices upgraded to software version 11) and Aisys CS2 anesthesia devices (GTIN: 840682102292) with PSVPro option and/or End Tidal Control option. |
| Affected: | |
| Software version: | |
| Recalling Organisation: | GE Healthcare Limited Level 7, Vero Centre 48 Shortland St Auckland 1010 |
| Contact Information: | 0800 659 465 |
| Manufacturer: | Datex-Ohmeda Inc |
| Issue: | The manufacturer has become aware that : Upgraded Aisys anesthesia devices (i.e. Aisys devices upgraded to software version 11) and Aisys CS2 anesthesia devices with End Tidal Control option (has the inability to set fresh gas settings) and/or PSVPro option (non-functional back-up ventilation after Cycling Procedure). |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 24/10/2018 |
