Philips Respironics, Inc. recalls

26 recalls on record · latest: March 2, 2026

Official U.S. recall history for Philips Respironics, Inc., compiled from official government records.

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Philips Respironics, Inc. recalls Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.

March 2, 2026 · Medical device recalls High risk In some situations, the Obstruction Alarm does not trigger within the timeframe…

Philips Respironics, Inc. recalls Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator device.

March 2, 2026 · Medical device recalls High risk In some situations, the Obstruction Alarm does not trigger within the timeframe…

Philips Respironics, Inc. recalls Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-use ventilator device.

March 2, 2026 · Medical device recalls High risk In some situations, the Obstruction Alarm does not trigger within the timeframe…

Philips Respironics, Inc. recalls Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.

March 2, 2026 · Medical device recalls High risk In some situations, the Obstruction Alarm does not trigger within the timeframe…

Philips Respironics, Inc. recalls Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.

March 2, 2026 · Medical device recalls High risk Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result…

Philips Respironics, Inc. recalls Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.

March 2, 2026 · Medical device recalls High risk Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result…

Philips Respironics, Inc. recalls Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator device.

March 2, 2026 · Medical device recalls High risk Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result…

Philips Respironics, Inc. recalls Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-use ventilator device.

March 2, 2026 · Medical device recalls High risk Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result…

Philips Respironics, Inc. recalls SimplyGo Mini, Standard Battery Kit; Product code: 1116816; The affected battery kits are sold as accessories for the S…

October 7, 2025 · Medical device recalls Moderate risk Certain serial numbers of the SimplyGo Mini standard battery kit contain a defe…

Philips Respironics, Inc. recalls DreamStation Auto CPAP. Non-Continuous Ventilator.

June 30, 2025 · Medical device recalls High risk Devices may possess a programming error resulting in an incorrect device config…

Philips Respironics, Inc. recalls DreamStation Auto. Non-Continuous Ventilator.

June 30, 2025 · Medical device recalls High risk Devices may possess a programming error resulting in an incorrect device config…

Philips Respironics, Inc. recalls DreamStation Auto BiPAP. Non-Continuous Ventilator.

June 30, 2025 · Medical device recalls High risk Devices may possess a programming error resulting in an incorrect device config…

Philips Respironics, Inc. recalls BiPAP A30 Ventilators. Intended to provide noninvasive ventilation support in adult and pediatric patients weighing mor…

May 9, 2025 · Medical device recalls High risk This device does not indicate for use in patients with respiratory failure.

Philips Respironics, Inc. recalls BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory support for pediatric and adult patients weighi…

May 9, 2025 · Medical device recalls High risk This device does not indicate for use in patients with respiratory failure.

Philips Respironics, Inc. recalls BiPAP A40 Ventilator. Used to provide noninvasive ventilation support for the purpose of treating adult and pediatric p…

May 9, 2025 · Medical device recalls High risk This device does not indicate for use in patients with respiratory failure.

Philips Respironics, Inc. recalls Philips Respironics — Trilogy Evo, Trilogy Evo O2, Trilogy Evo Universal, and Trilogy EV300 ventilators

October 7, 2024 · Medical device recalls The use of in-line nebulizers placed in certain locations may lead to aerosol d…

Philips Respironics, Inc. recalls Trilogy Evo. Model Numbers: DS2110X11B, UDS2110X11B, RDS2110X11B, CA2110X12B, JP2110X16B, IN2110X15B, DE2110X13B, AU211…

October 7, 2024 · Medical device recalls High risk Potential for in-line nebulizer configuration in certain locations to result in…

Philips Respironics, Inc. recalls Trilogy Evo O2. Model Numbers: FP2100X10, DS2100X11B, IN2100X15B, DE2100X13B, IA2100X15B, EU2100X15B, LA2100X15B, EE210…

October 7, 2024 · Medical device recalls High risk Potential for in-line nebulizer configuration in certain locations to result in…

Philips Respironics, Inc. recalls LifeVent EVO2. Model Number: SP2100X26B. Intended for invasive and non-invasive ventilation of pediatric through adult…

October 7, 2024 · Medical device recalls High risk Potential for in-line nebulizer configuration in certain locations to result in…

Philips Respironics, Inc. recalls Garbin Evo. Model Number: LD2110X23B. Intended for invasive and non-invasive ventilation of pediatric through adult pat…

October 7, 2024 · Medical device recalls High risk Potential for in-line nebulizer configuration in certain locations to result in…

Philips Respironics, Inc. recalls Aeris EVO. Model Number: VT2110X24B. Intended for invasive and non-invasive ventilation of pediatric through adult pati…

October 7, 2024 · Medical device recalls High risk Potential for in-line nebulizer configuration in certain locations to result in…

Philips Respironics, Inc. recalls Trilogy EV300. Model Numbers: DS2200X11B, IN2200X15B, BL2200X15B, BR2200X18B, CA2200X12B, DE2200X13B, GB2200X15B, ND220…

October 7, 2024 · Medical device recalls High risk Potential for in-line nebulizer configuration in certain locations to result in…

Philips Respironics, Inc. recalls Trilogy Evo Universal Ventilator. Model Number DS2000X11B. Intended for invasive and non-invasive ventilation of pediat…

October 7, 2024 · Medical device recalls High risk Potential for in-line nebulizer configuration in certain locations to result in…

Philips Respironics, Inc. recalls Trilogy Evo EV300 -- Model Number/ Model Description: BL2200X15B Trilogy Evo, O2, Benelux EV300; BR2200X18B Trilogy Evo…

July 16, 2024 · Medical device recalls High risk Firm has released a mandatory software update Version 1.05.10.00 and a User Man…

Philips Respironics, Inc. recalls Trilogy Evo Universal Ventilator, Model No. DS2000X11B

July 16, 2024 · Medical device recalls High risk Firm has released a mandatory software update Version 1.05.10.00 and a User Man…

Philips Respironics, Inc. recalls Trilogy Evo; Model No./Model Description -- AU2110X15B Trilogy Evo, Australia BL2110X15B Trilogy Evo, Benelux BR2110X18…

July 16, 2024 · Medical device recalls High risk Firm has released a mandatory software update Version 1.05.10.00 and a User Man…