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
April 1, 2026FDAPhilips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use venti…Z-1616-2026
April 1, 2026FDAPhilips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-u…Z-1617-2026
July 9, 2025FDABiPAP A40 Ventilator. Used to provide noninvasive ventilation support for the purpose of …Z-2037-2025
November 20, 2024FDATrilogy EV300. Model Numbers: DS2200X11B, IN2200X15B, BL2200X15B, BR2200X18B, CA2200X12B,…Z-0293-2025
November 20, 2024FDATrilogy Evo O2. Model Numbers: FP2100X10, DS2100X11B, IN2100X15B, DE2100X13B, IA2100X15B,…Z-0290-2025
November 20, 2024FDATrilogy Evo Universal Ventilator. Model Number DS2000X11B. Intended for invasive and non…Z-0292-2025
November 20, 2024FDALifeVent EVO2. Model Number: SP2100X26B. Intended for invasive and non-invasive ventilat…Z-0296-2025
November 20, 2024FDAAeris EVO. Model Number: VT2110X24B. Intended for invasive and non-invasive ventilation…Z-0294-2025
November 20, 2024FDATrilogy Evo. Model Numbers: DS2110X11B, UDS2110X11B, RDS2110X11B, CA2110X12B, JP2110X16B,…Z-0291-2025
November 20, 2024FDAGarbin Evo. Model Number: LD2110X23B. Intended for invasive and non-invasive ventilatio…Z-0295-2025
September 11, 2024FDATrilogy Evo; Model No./Model Description -- AU2110X15B Trilogy Evo, Australia BL211…Z-2944-2024
September 11, 2024FDATrilogy Evo EV300 -- Model Number/ Model Description: BL2200X15B Trilogy Evo, O2, Benel…Z-2942-2024
September 11, 2024FDATrilogy Evo Universal Ventilator, Model No. DS2000X11BZ-2943-2024
May 29, 2024FDAOmniLab Advanced + Ventilator Product Numbers 1111122 1111123 1111124 1111125 111112…Z-1817-2024
May 29, 2024FDABiPAP A40 Ventilators: BiPAP A40, Part Numbers 1111169 (US and OUS) and (OUS ONLY)1…Z-1813-2024
May 29, 2024FDABiPAP A30 Ventilator, Part Number 1111143 (US and OUS) OUS Only: Part Numbers 1111144…Z-1814-2024
May 29, 2024FDABiPAP V30 Auto Ventilator, Part Number 1111178Z-1812-2024
April 24, 2024FDAGarbin EVO, all software versions except 1.05.06.00. Ventilator for pediatric and adult p…Z-1500-2024
April 24, 2024FDALifeVentEVO2, all software versions except 1.05.06.00. Ventilator for pediatric and adult…Z-1501-2024
April 24, 2024FDATrilogy Evo O2, all software versions except 1.05.06.00. Ventilator for pediatric and adu…Z-1503-2024
April 24, 2024FDATrilogy Evo, all software versions except 1.05.06.00. Ventilator for pediatric and adult …Z-1504-2024
April 24, 2024FDATrilogy Evo Universal Ventilator, all software versions except 1.05.06.00. Ventilator for…Z-1505-2024
April 24, 2024FDAAeris EVO, all software versions except 1.05.06.00. Ventilator for pediatric and adult pa…Z-1499-2024
April 24, 2024FDATrilogy EV300, all software versions except 1.05.06.00. Ventilator for pediatric and adul…Z-1502-2024
January 10, 2024FDATrilogy Evo and Trilogy Evo O2 Material Numbers BL2110X15B BR2110X18B CA2110X12B DE21…Z-0638-2024

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.
What was the most recent Philips Respironics, Inc. recall?
FDA recall Z-1616-2026, published April 1, 2026: Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator device.
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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