Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 29151 |
| Brand Name: | Alternating Systems – Auralis, Nimbus, AtmosAir, Alpha Active, Alpha Response, Alpha Trancell, Auto Logic, Bari Breeze, Therakair Visio mattresses & seat cushions |
| Model: | |
| Affected: | Auralis software upgrade to V1.3.0.1 |
| Software version: | |
| Recalling Organisation: | Arjo New Zealand Limited 34 Vestey Drive Mt Wellington AUCKLAND 1060 |
| Contact Information: | 0800 000 151 |
| Manufacturer: | ArjoHuntleigh AB |
| Issue: | The manufacturer has identified that Auralis pumps might fail causing an abnormal level of noise emitted and low pressure alarm being triggered. Following the manufacturer investigation, it has been confirmed that the issue occurs due to a software fault in the pump that makes the compressor working uncontrolled (out of its specified tolerance) and generating the high level of noise. This, in turn, leads to the premature wear of that part. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 23/3/2022 |
