BiPAP A40, DreamStation, BiPAP A30, BiPAP Auto System One 60 Series, BiPAP AVAPS C Series, BiPAP A40 Pro, Trilogy Evo, REMstar, SIMPLYGO and Elegance devices
Published 20 December 2022
Product
The product list was updated on 1 February 2023 to include additional models. This recall covers models with power cords that do not comply with requirements in the Medical electrical equipment standard IEC60601-1. This is separate to recall PRA 2021/19121 - Philips Electronics Australia Ltd — Philips Respironics - Certain CPAP and Bi-Level PAP Devices Philips Respironics – Sleep & Respiratory Care Devices BiPAP A40 DreamStation BiPAP A30 BiPAP Auto System One 60 Series BiPAP AVAPS C Series BiPAP A40 Pro BiPAP A40 EFL Trilogy Evo REMstar SIMPLYGO Elegance devices ARTG's 200289, 295664, 133794, 209934, 329407 329408, 295664, 274181, 278352 See attached product list
Why it was recalled
The power cord supplied in affected products does not comply with requirements in the Medical electrical equipment standard IEC60601-1.
Hazard
The power cord supplied may not withstand humidity and mechanical stresses to the same level of the required cord.
Source: Product Safety Australia. RecallMatch AU provides a screening summary and is independent of the ACCC.