Garbin Plus, Aeris, LifeVent (Ventilator)Ī-Series BiPAP Hybrid A30 (not marketed in US)Ī-Series BiPAP A30 (not marketed in US) What if I have an affected device? OmniLab Advanced Plus (In-Lab Titration Device)Īll Affected Devices Manufactured Before 26 April 2021, All Device Serial Numbers However, the affected devices are common to many DME distributors, according to the Philips website the affected CPAP and BiLevel PAP devices are:Īll Affected Devices Manufactured Before 26 April 2021, All Device Serial Numbers:Ĭontinuous Ventilator, Minimum Ventilatory Support, Facility UseĬontinuous Ventilator, Non-life Supporting The affected devices are not ones that we distribute through our in-house durable medical equipment department. For information on the Recall Notice, a complete list of impacted products, and potential health risks, visit /src-update.
Philips Respironics announced a voluntary recall for Continuous and Non-Continuous Ventilators (certain CPAP, BiLevel PAP and Ventilator Devices) due to two issues related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in these devices. Expert Sleep Medicine was recently made aware of an ongoing voluntary recall of certain Philips Respironics devices:
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