Philips Respironics, Inc. recalls
Every recall we track for Philips Respironics, Inc. — 93 in all, from 2018–2026 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from Philips Respironics, Inc. fell by more than half in 2025 (7, down from 21 in 2024). 1% rated “stop using now”.
All FDA recall records for Philips Respironics, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 1 | 0 | 1 |
| 2019 | 0 | 13 | 0 | 0 | 13 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 10 | 4 | 4 | 18 |
| 2022 | 0 | 2 | 12 | 0 | 14 |
| 2023 | 0 | 5 | 5 | 1 | 11 |
| 2024 | 1 | 10 | 10 | 0 | 21 |
| 2025 | 0 | 2 | 5 | 0 | 7 |
| 2026 (to date) | 0 | 4 | 4 | 0 | 8 |
Most common reasons for Philips Respironics, Inc. recalls
What to do if you have a recalled Philips Respironics, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Philips Respironics, Inc. recalls
26 shown- Use cautionMedical device
Philips Respironics, Inc. recalls Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.
Philips Respironics recalls Trilogy Evo O2 ventilators with software version 1.05.15.00 due to potential obstruction alarm failure. Affected units may not trigger alarms within standard timeframes, risking breathing issues.
Philips RespironicsMar 2, 2026 - Use cautionMedical device
Philips Respironics, Inc. recalls Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-use ventilator device.
Philips Respironics recalls Trilogy Evo Universal ventilators with software version 1.05.15.00 due to potential tidal volume mismatch when using non-pneumatic nebulizers. Affected units may require software update or device check.
Philips RespironicsMar 2, 2026 - Use cautionMedical device
Philips Respironics, Inc. recalls SimplyGo Mini, Standard Battery Kit; Product code: 1116816; The affected battery kits are sold as accessories for the
Philips Respironics recalls SimplyGo Mini standard battery kits with defective chips that can cause oxygen shutdown during use. Affected units have specific serial numbers and may be sold as accessories for portable oxygen concentrators.
Philips RespironicsOct 7, 2025 - Use cautionMedical device
Philips Respironics, Inc. recalls DreamStation Auto BiPAP. Non-Continuous Ventilator.
Philips Respironics recalls a small number of DreamStation Auto BiPAP non-continuous ventilators due to a programming error causing incorrect device configuration.
Philips RespironicsJun 30, 2025 - Lower riskMedical device
Philips Respironics, Inc. recalls BiPAP A40 Ventilator. Used to provide noninvasive ventilation support for the purpose of treating adult and pediatric
Philips Respironics recalls BiPAP A40 Ventilators that are not indicated for use in patients with respiratory failure. Affected units have specific serial numbers. Consumers should stop using if they have the device and contact Philips for details.
Philips RespironicsMay 9, 2025 - Lower riskMedical device
Philips Respironics, Inc. recalls Trilogy Evo Universal Ventilator. Model Number DS2000X11B. Intended for invasive and non-invasive ventilation of
Philips Respironics recalls Trilogy Evo Universal Ventilators (model DS2000X11B) due to potential inaccurate flow measurements from aerosol deposits. Affected units may require servicing to prevent incorrect ventilation readings.
Philips RespironicsOct 7, 2024 - Lower riskMedical device
Philips Respironics, Inc. recalls Trilogy Evo; Model No./Model Description -- AU2110X15B Trilogy Evo, Australia BL2110X15B Trilogy Evo, Benelux
Philips Respironics recalls Trilogy Evo ventilators with specific model numbers for safety software updates. Affected units require a software update to resolve identified safety issues.
Philips RespironicsJul 16, 2024 - Stop using nowMedical device
Philips Respironics, Inc. recalls OmniLab Advanced + Ventilator Product Numbers 1111122 1111123 1111124 1111125 1111126 1111127 1111138 1111141 1111142
Philips Respironics recalls specific OmniLab Advanced ventilator models (product numbers 1111122-1111142) due to potential interruption of therapy, which may lead to hypoventilation, hypoxemia, hypercarbia, respiratory failure, or death.
Philips RespironicsApr 1, 2024 - Use cautionMedical device
Philips Respironics, Inc. recalls BiPAP V30 Auto Ventilator, Part Number 1111178
Philips Respironics recalls BiPAP V30 Auto Ventilator (Part Number 1111178) due to potential interruption of therapy during Ventilator Inoperative alarms, which may lead to hypoventilation, hypoxemia, hypercarbia, respiratory failure, or death in vulnerable patients.
Philips RespironicsMar 26, 2024 - Use cautionMedical device
Philips Respironics, Inc. recalls Trilogy Evo Universal Ventilator, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients.
Philips Respironics recalls all Trilogy Evo Universal Ventilators except software version 1.05.06.00 due to potential sudden loss of ventilation from battery or power alarms.
Philips RespironicsMar 19, 2024 - Use cautionMedical device
Philips Respironics, Inc. recalls Trilogy Evo and Trilogy Evo O2 Material Numbers BL2110X15B BR2110X18B CA2110X12B DE2100X13B DE2110X13B DS2100X11B
Philips Respironics recalls Trilogy Evo and Trilogy Evo O2 devices with specific material numbers. These devices may cause barotrauma or breathing issues if used on patients under 10 kg due to missing contraindications in the safety statement.
Philips RespironicsNov 27, 2023 - Use cautionMedical device
Philips Respironics, Inc. recalls Philips Respironics V60/V60 Plus Ventilator, PCBA Part Number: 453561544461 V60 Device Part Numbers 1053617 (US) and
Philips Respironics recalls V60/V60 Plus ventilators with specific PCBA part numbers due to potential power failure causing loss of function. Affected units may need replacement.
Philips RespironicsAug 25, 2023 - Lower riskMedical device
Philips Respironics, Inc. recalls Trilogy Evo, Evo Clinical Korean (1137823) and Evo Caregiver Korean (1137853) Instructions for Use
Philips Respironics recalls Korean instructions for use for Trilogy Evo, Evo Clinical and Evo Caregiver models due to incorrect translation of 'invasive' as 'noninvasive' in the instructions.
Philips RespironicsMay 25, 2023 - Lower riskMedical device
Philips Respironics, Inc. recalls Trilogy Evo O2 EV300, Model Numbers DS2200X11B, IN2200X15B, FX2200X15B, CA2200X12B, FR2200X14B, ND2200X15B, ES2200X15B,
Philips Respironics is a leading manufacturer of medical devices, including ventilators, monitors, and other respiratory care products.
Philips RespironicsMay 1, 2023 - Lower riskMedical device
Philips Respironics, Inc. recalls Trilogy EV300 Portable Electric Ventilator, Model Numbers DS2200X11B, IN2200X15B, FX2200X15B, CA2200X12B, CN2200X17B,
Philips Respironics recalls Trilogy EV300 Portable Electric Ventilators with specific model numbers due to potential oxygen delivery inaccuracies below required tolerance, which could lead to under-delivery of oxygen during high concentration therapy.
Philips RespironicsMar 1, 2023 - Lower riskMedical device
Philips Respironics, Inc. recalls Philips DreamStation Auto BiPAP and CPAP, Model Numbers UCDSX500S11, UDSX500S11, UDSX500S11F, UDSX700S11, UDSX700S11F,
Philips recalls limited DreamStation Auto BiPAP and CPAP units with model numbers UCDSX500S11, UDSX500S11, etc. for potential cloud communication issues that could cause incorrect prescription settings or inability to download settings. Affected units may need verification.
PhilipsFeb 10, 2023 - Lower riskMedical device
Philips Respironics, Inc. recalls Philips Trilogy 100 Ventilator, Model Numbers 1054260, 1054096, U1054260, U1054260B, 1054260B, CA1054096B, BT1054260,
Philips Respironics recalls certain Trilogy 100 Ventilators where replacement silicone sound abatement foam may separate from plastic backing, potentially reducing therapy volume or causing alarms. Affected models include 1054260, 1054096, U1054260, and others. No immediate action needed but check your device.
Philips RespironicsDec 7, 2022 - Lower riskMedical device
Philips Respironics, Inc. recalls Wisp and Wisp Youth Nasal Mask
Philips Respironics recalls Wisp and Wisp Youth Nasal Masks due to no known magnetic risks for patients with implantable devices or metallic splinters in eyes. All units are affected.
Philips RespironicsSep 6, 2022 - Lower riskMedical device
Philips Respironics, Inc. recalls Philips BiPAP A30, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea
Philips recalls BiPAP A30 devices with nonconforming plastic that may off-gas VOCs. Affected units have specific model and serial numbers. Contact Philips for details.
Philips RespironicsAug 26, 2022 - Use cautionMedical device
Philips Respironics, Inc. recalls Trilogy Evo, Material Numbers DS2110X11B (USA) and KR2110X15B (Korea) The Trilogy Evo ventilator provides continuous or
Philips Respironics recalls Trilogy Evo ventilators with specific material numbers due to non-conforming sound abatement foam that may degrade into particles and be inhaled by users.
Philips RespironicsDec 22, 2021 - UnratedMedical device
Philips Respironics, Inc. recalls Trilogy Evo Universal, Product number DS2000X11B
Philips Respironics recalls Trilogy Evo Universal devices with specific software versions due to potential pressure increases in infants and children. Affected units may require software updates to prevent risks.
Philips RespironicsJul 26, 2021 - UnratedMedical device
Philips Respironics, Inc. recalls Philips Respironics E30 with Humidifier, Continuous Ventilator, Minimum Ventilatory Support, Facility Use; Product
Philips Respironics recalls E30 ventilators with humidifier due to potential foam particles entering airways. Affected models include DSX9999H11, INX9999H19, RINX9999H19. No remedy specified in recall notice.
Philips RespironicsJun 14, 2021 - Use cautionMedical device
Philips Respironics, Inc. recalls Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent Continuous Ventilators.
Philips Respironics recalls Trilogy 100, 200, Garbin Plus, Aeris, and LifeVent ventilators made before April 2021 due to potential PE-PUR foam particles entering air pathways and being inhaled or ingested by users.
Philips RespironicsJun 14, 2021 - Use cautionMedical device
Philips Respironics, Inc. recalls BiPAP A40 System Silver, JP: Continuous ventilator, non-life-supporting. Material Number: R1111177
Philips Respironics recalls BiPAP A40 System Silver ventilators due to potential VOC exposure from non-conforming plastic. Affected units may fail suddenly, risking asphyxia if not addressed by care providers.
Philips RespironicsApr 6, 2021 - Use cautionMedical device
Philips Respironics, Inc. recalls Trilogy EVO Ventilator, Nordics - Model Number: ND2110X15B Trilogy Evo is intended for pediatric through adult patients
Philips Respironics recalls Trilogy EVO Ventilators with specific software versions due to power alarm failure risk. Affected models include ND2110X15B with serial numbers listed. This defect may cause loss of critical safety alerts.
Philips RespironicsNov 19, 2019 - Lower riskMedical device
Philips Respironics, Inc. recalls Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent Continuous Ventilators The device is intended to be used in
Philips Respironics recalls Trilogy 100, Trilogy 200, Garbin Plus, Aeris, and LifeVent ventilators due to potential foam degradation. Affected units may need replacement to prevent particle release.
Philips RespironicsJun 12, 2018
Philips Respironics, Inc. recall questions
How many recalls has Philips Respironics, Inc. had?
93 recalls from Philips Respironics, Inc. are on record with U.S. safety agencies, from 2018–2026.
What is the most recent Philips Respironics, Inc. recall?
Philips Respironics, Inc. recalls Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device., dated Mar 2, 2026. Every Philips Respironics, Inc. recall is listed on this page, newest first.
Why are Philips Respironics, Inc. products recalled?
The most common reasons on record: This device does not indicate for use in patients with respiratory failure. (3).
What should I do if I have a recalled Philips Respironics, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Philips Respironics, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.