Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 28095 |
| Brand Name: | Anaesthesia Work Stations |
| Model: | |
| Affected: | Affected Flow sensor - 2089610-001-(S), 2087640-001, 2096513-001-S, 5697309 R-FMI34109, 5697310 R-FMI34109 |
| 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 identified that a small number of flow sensors built prior to June 2021 could have damaged tubes with small punctures or cuts. This issue could cause leaks resulting in incorrect anesthesia machine tidal volumes, potentially leading to over-delivery of volume to the patient. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 27/7/2021 |
