Philips Respironics, Inc.: A-Series BiPAP Hybrid A30 (not marketed in US),
Recall reason: The polyester-based polyurethane (PE-PUR) foam may degrade into particles which may enter the devices air pathway and be ingested or inhaled by the user, and the PE-PUR foam may off-gas certain chemicals.. Recalled by Philips Respironics, Inc.. Distribution: Worldwide distribution including US Nationwide, Argentina, Australia, Brazil, Canada, China, France, Germany, Italy, Japan, Korea, and Latin America.. Classification (Class I — serious health hazard). Affected lots/dates: All Devices manufactured before 26 April 2021, All device serial numbers. Material Numbers 1111181 1111182 1111178. Contact the manufacturer or the retailer where you purchased this device to arrang
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