Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:27105
Brand Name:Alternating Systems - AtmosAir, Nimbus, Alpha, Active, Response, Logic and Trancell Ranges. Bari Breeze and Autologic 110 & 200; Therakair Visio; Auralis Mattresses & Seat Cushion
Model:
Affected:
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 investigated customer complaints where mains cables have been damaged accidently or through miss-use (i.e. incorrectly stowed). Although the mains cables on the Alpha Active models listed have been tested to, and comply with IEC60601-1 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance, and are fit for purpose, the investigation has identified ways of mitigating possible damage by increasing the cable wall thickness and incorporating an improved grommet.
Recall action type:Correction
Recall action:Manufacturer to issue advice regarding use
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:23/12/2020
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