Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 24383 |
| Brand Name: | Anaesthesia Work Stations |
| Model: | |
| Affected: | All upgraded Aisys anesthesia devices (i.e. Aisys devices upgraded to software version 11SP01 or 11SP02) and Aisys CS2 anesthesia devices with software version 11SP01 or 11SP02 (GTIN: 840682102292) and Et Control option |
| 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 : Aisys CS2 anesthesia devices with software version 11 and Aisys anesthesia devices upgraded to software version 11 with End Tidal Control option (when Et Control auto-exits during Pause Gas procedure agent delivery is off and fresh gas total flow is 10 L/min, resulting in the agent concentration quickly decreasing). |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 1/4/2019 |
