Philips Respironics, Inc.: 39 recalls on record

Recalls filed with 1 agency: FDA (39).

First recall on record: February 26, 2020. Most recent: April 1, 2026.

Risk classification: Class I: 37 · Class II: 2

Most recent recalls

DateAgencyProduct
October 4, 2023FDAPhilips Respironics V60/V60 Plus Ventilator, PCBA Part Number: 453561544461 V60 De…Z-2631-2023
June 14, 2023FDATrilogy Evo O2 EV300, Model Numbers DS2200X11B, IN2200X15B, FX2200X15B, CA2200X12B, FR220…Z-1651-2023
October 12, 2022FDAWisp and Wisp Youth Nasal MaskZ-1783-2022
October 12, 2022FDADreamWisp Nasal Mask with Over the Nose CushionZ-1782-2022
September 14, 2022FDAPhilips BiPAP A30, Rx Only. To provide noninvasive ventilation support for patients with…Z-1654-2022
February 2, 2022FDATrilogy Evo, Material Numbers DS2110X11B (USA) and KR2110X15B (Korea) The Trilogy Evo …Z-0493-2022
August 25, 2021FDATrilogy Evo Universal, Product number DS2000X11BZ-2290-2021
July 21, 2021FDATrilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent Continuous Ventilators.Z-1956-2021
February 26, 2020FDATrilogy EVO Ventilator, France - Model Number: FR2110X14B Trilogy Evo is intended for …Z-0949-2020
February 26, 2020FDAGarbin EVO Ventilator, Linde - Model Number: LD2110X23B Trilogy Evo is intended for pe…Z-0946-2020
February 26, 2020FDATrilogy EVO Ventilator, Nordics - Model Number: ND2110X15B Trilogy Evo is intended for…Z-0948-2020
February 26, 2020FDATrilogy EVO Ventilator, Iberia - Model Number: ES2110X15B Trilogy Evo is intended for …Z-0943-2020
February 26, 2020FDATrilogy EVO Ventilator, EU - Model Number: EU2110X15B Trilogy Evo is intended for pedi…Z-0945-2020
February 26, 2020FDALifeVent EVO Ventilator, 02 - Model Number: SP2100X26B Trilogy Evo is intended for ped…Z-0954-2020

Questions about this company

How many recalls does Philips Respironics, Inc. have?
Recalert has 39 U.S. recalls on record for Philips Respironics, Inc., published between February 26, 2020 and April 1, 2026.
Which agencies have handled Philips Respironics, Inc. recalls?
Philips Respironics, Inc. appears as the recalling firm in recalls from: FDA (39).

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