Philips Respironics recalls

Philips Respironics has 76 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 8 Apr 2026. 56 are still ongoing. 9 were reported in the last 12 months. The most frequent reason is device malfunction.

Total recalls76since 2016
Last 12 months9reported
Class I6282% of total
Ongoing56latest 8 Apr 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 62 82%Class II 14 18%Class III 0 0%

By year

Ongoing philips respironics recalls

56 active

All philips respironics recalls, newest first

76 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS ITrilogy Evo recalled by Philips RespironicsPhilips RespironicsDevice MalfunctionNationwide
DeviceCLASS ITrilogy EV300 recalled by Philips RespironicsPhilips RespironicsDevice MalfunctionNationwide
DeviceCLASS ITrilogy Evo Universal recalled by Philips RespironicsPhilips RespironicsDevice MalfunctionNationwide
DeviceCLASS ITrilogy Evo O2 recalled by Philips RespironicsPhilips RespironicsDevice MalfunctionNationwide
DeviceCLASS ITrilogy Evo recalled by Philips RespironicsPhilips RespironicsDevice MalfunctionNationwide
DeviceCLASS ITrilogy Evo O2 recalled by Philips RespironicsPhilips RespironicsDevice MalfunctionNationwide
DeviceCLASS ITrilogy EV300 recalled by Philips RespironicsPhilips RespironicsDevice MalfunctionNationwide
DeviceCLASS ITrilogy Evo Universal recalled by Philips RespironicsPhilips RespironicsDevice MalfunctionNationwide
DeviceCLASS IISimplyGo Mini, Standard Battery Kit recalled by Philips RespironicsPhilips RespironicsTemperature AbuseNationwide
DeviceCLASS IDreamStation Auto CPAP recalled by Philips RespironicsPhilips RespironicsOtherNationwide
DeviceCLASS IDreamStation Auto recalled by Philips RespironicsPhilips RespironicsOtherNationwide
DeviceCLASS IDreamStation Auto BiPAP recalled by Philips RespironicsPhilips RespironicsOtherNationwide
DeviceCLASS ITrilogy Evo recalled by Philips RespironicsPhilips RespironicsLabeling ErrorsNationwide
DeviceCLASS ITrilogy Evo O2 recalled by Philips RespironicsPhilips RespironicsLabeling ErrorsNationwide
DeviceCLASS ILifeVent EVO2 recalled by Philips RespironicsPhilips RespironicsLabeling ErrorsNationwide
DeviceCLASS IGarbin Evo recalled by Philips RespironicsPhilips RespironicsLabeling ErrorsNationwide
DeviceCLASS IAeris EVO recalled by Philips RespironicsPhilips RespironicsLabeling ErrorsNationwide
DeviceCLASS ITrilogy EV300 recalled by Philips RespironicsPhilips RespironicsLabeling ErrorsNationwide
DeviceCLASS ITrilogy Evo Universal Ventilator recalled by Philips RespironicsPhilips RespironicsLabeling ErrorsNationwide
DeviceCLASS ITrilogy Evo, all recalled by Philips RespironicsPhilips RespironicsDevice MalfunctionNationwide
DeviceCLASS IGarbin EVO, all recalled by Philips RespironicsPhilips RespironicsDevice MalfunctionNationwide
DeviceCLASS ITrilogy EV300, all recalled by Philips RespironicsPhilips RespironicsDevice MalfunctionNationwide
DeviceCLASS ITrilogy Evo O2, all recalled by Philips RespironicsPhilips RespironicsDevice MalfunctionNationwide
DeviceCLASS IAeris EVO, all recalled by Philips RespironicsPhilips RespironicsDevice MalfunctionNationwide
DeviceCLASS ILifeVentEVO2, all recalled by Philips RespironicsPhilips RespironicsDevice MalfunctionNationwide
DeviceCLASS ITrilogy Evo Universal Ventilator, all recalled by Philips RespironicsPhilips RespironicsDevice MalfunctionNationwide
DeviceCLASS IITrilogy Evo and Trilogy Evo O2 Material Numbers BL2110X15B recalledPhilips RespironicsOtherNationwide
DeviceCLASS IV60/V60 Plus Ventilator, PCBA recalled by Philips RespironicsPhilips RespironicsDevice Malfunction4 states
DeviceCLASS IITrilogy Evo, Evo Clinical Korean (1137823) recalledPhilips RespironicsOtherPA
DeviceCLASS IPhilips DreamStation Auto BiPAP and CPAP recalled by Philips RespironicsPhilips RespironicsOtherNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.