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Philips Respironics, Inc.

Philips Respironics, Inc. Recalls

All product recalls associated with Philips Respironics, Inc..

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Recall Summary

Total Recalls

139

Past Year

7

Class I (Serious)

1

Most Recent

Oct 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–20 of 139 recalls

SimplyGo Mini Battery Kit (Philips) – charging defect (2025)

Certain serial numbers of the SimplyGo Mini standard battery kit contain a defective chip which can lead the battery to either fail to charge or lose voltage output when in use in the device. If the fault occurs while the device is running on battery power, the SimplyGo Mini will shut down and stop providing oxygen to the user. This may happen at a temperature within the specified operating temperature range of the SimplyGo Mini.

FDAOct 7, 2025Nationwide• Philips Respironics, Inc.

DreamStation Auto (Philips Respironics) – Configuration Error (2025)

Devices may possess a programming error resulting in an incorrect device configuration.

FDAJun 30, 2025Nationwide• Philips Respironics, Inc.

DreamStation Auto CPAP (Philips Respironics) – Configuration Error (2025)

Devices may possess a programming error resulting in an incorrect device configuration.

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FDAJun 30, 2025Nationwide• Philips Respironics, Inc.

DreamStation Auto BiPAP (Philips Respironics) – Configuration Error (2025)

Devices may possess a programming error resulting in an incorrect device configuration.

FDAJun 30, 2025Nationwide• Philips Respironics, Inc.

BiPAP A40 Ventilator (Philips) – Usage Limitation (2025)

This device does not indicate for use in patients with respiratory failure.

FDAMay 9, 2025Nationwide• Philips Respironics, Inc.

BiPAP V30 Ventilator (Philips) – Usage Limitation (2025)

This device does not indicate for use in patients with respiratory failure.

FDAMay 9, 2025Nationwide• Philips Respironics, Inc.

BiPAP A30 Ventilators (Philips) – Usage Limitation (2025)

This device does not indicate for use in patients with respiratory failure.

FDAMay 9, 2025Nationwide• Philips Respironics, Inc.

Garbin Evo Ventilator (Philips) – Nebulizer Flow Sensor Issue (2024)

Potential for in-line nebulizer configuration in certain locations to result in aerosol deposit accumulation on the device's internal flow sensor, which could lead to inaccurate flow measurements.

FDAOct 7, 2024Nationwide• Philips Respironics, Inc.

Trilogy Evo Universal Ventilator (Philips) – Nebulizer Flow Sensor Issue (2024)

Potential for in-line nebulizer configuration in certain locations to result in aerosol deposit accumulation on the device's internal flow sensor, which could lead to inaccurate flow measurements.

FDAOct 7, 2024Nationwide• Philips Respironics, Inc.

Trilogy EV300 Ventilator (Philips) – Nebulizer Flow Sensor Issue (2024)

Potential for in-line nebulizer configuration in certain locations to result in aerosol deposit accumulation on the device's internal flow sensor, which could lead to inaccurate flow measurements.

FDAOct 7, 2024Nationwide• Philips Respironics, Inc.

Trilogy Evo O2 Ventilator (Philips) – Nebulizer Flow Sensor Issue (2024)

Potential for in-line nebulizer configuration in certain locations to result in aerosol deposit accumulation on the device's internal flow sensor, which could lead to inaccurate flow measurements.

FDAOct 7, 2024Nationwide• Philips Respironics, Inc.

Aeris EVO Ventilator (Philips) – Nebulizer Flow Sensor Issue (2024)

Potential for in-line nebulizer configuration in certain locations to result in aerosol deposit accumulation on the device's internal flow sensor, which could lead to inaccurate flow measurements.

FDAOct 7, 2024Nationwide• Philips Respironics, Inc.

Trilogy Evo Ventilator (Philips) – Nebulizer Flow Sensor Issue (2024)

Potential for in-line nebulizer configuration in certain locations to result in aerosol deposit accumulation on the device's internal flow sensor, which could lead to inaccurate flow measurements.

FDAOct 7, 2024Nationwide• Philips Respironics, Inc.

LifeVent EVO2 Ventilator (Philips) – Nebulizer Flow Sensor Issue (2024)

Potential for in-line nebulizer configuration in certain locations to result in aerosol deposit accumulation on the device's internal flow sensor, which could lead to inaccurate flow measurements.

FDAOct 7, 2024Nationwide• Philips Respironics, Inc.

Trilogy Evo EV300 -- Model Number/ Model Description: BL2... (Philips Respironics, Inc.) – firm has released a mandatory softwar... (2024)

Firm has released a mandatory software update Version 1.05.10.00 and a User Manual addendum for affected ventilators. These updates resolve safety issues identified in earlier recalls.

FDAJul 16, 2024Nationwide• Philips Respironics, Inc.

Trilogy Evo; Model No./Model Description -- AU2110X15B ... (Philips Respironics, Inc.) – firm has released a mandatory softwar... (2024)

Firm has released a mandatory software update Version 1.05.10.00 and a User Manual addendum for affected ventilators. These updates resolve safety issues identified in earlier recalls.

FDAJul 16, 2024Nationwide• Philips Respironics, Inc.

Trilogy Evo Universal Ventilator, Model No. DS2000X11B (Philips Respironics, Inc.) – firm has released a mandatory softwar... (2024)

Firm has released a mandatory software update Version 1.05.10.00 and a User Manual addendum for affected ventilators. These updates resolve safety issues identified in earlier recalls.

FDAJul 16, 2024Nationwide• Philips Respironics, Inc.

Philips Respironics, Inc.: OmniLab Advanced + Ventilator Product Numbers 1111122 1...

Device may experience an interruption or loss of therapy in case of a Ventilator Inoperative alarm. This may lead to hypoventilation, mild to severe hypoxemia, hypercarbia, respiratory failure/insufficiency, or potentially death.

FDAApr 1, 2024Nationwide• Philips Respironics, Inc.

Philips Respironics, Inc.: BiPAP A30 Ventilator, Part Number 1111143 (US and OUS) OU...

Potential for devices to experience interruption/loss of therapy during a Ventilator Inoperative alarm. This may lead to hypoventilation, mild to severe hypoxemia, hypercarbia, respiratory failure/insufficiency, or potentially death in the most vulnerable patients.

FDAMar 26, 2024Nationwide• Philips Respironics, Inc.

Philips Respironics, Inc.: BiPAP V30 Auto Ventilator, Part Number 1111178

Potential for devices to experience interruption/loss of therapy during a Ventilator Inoperative alarm. This may lead to hypoventilation, mild to severe hypoxemia, hypercarbia, respiratory failure/insufficiency, or potentially death in the most vulnerable patients.

FDAMar 26, 2024Nationwide• Philips Respironics, Inc.