PlainRecalls

Philips Respironics, Inc.

58 recalls on record · Latest: Nov 19, 2025

Philips Respironics, Inc. Recall Insight

Philips Respironics, Inc. appears on 58 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.069% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Nov 19, 2025, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 41 critical, 9 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Feb 26, 2020 to Nov 19, 2025.

Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Nov 19, 2025

SimplyGo Mini, Standard Battery Kit; Product code: 1116816; The affected battery kits are sold as accessories for the SimplyGo Mini: SimplyGo Mi…

FDA Devices Critical Aug 20, 2025

DreamStation Auto BiPAP. Non-Continuous Ventilator.

FDA Devices Critical Aug 20, 2025

DreamStation Auto. Non-Continuous Ventilator.

FDA Devices Critical Aug 20, 2025

DreamStation Auto CPAP. Non-Continuous Ventilator.

FDA Devices Critical Jul 9, 2025

BiPAP A40 Ventilator. Used to provide noninvasive ventilation support for the purpose of treating adult and pediatric patients. BiPAP A40 Pro - sol…

FDA Devices Critical Jul 9, 2025

BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory support for pediatric and adult patients weighing over 10 kg.

FDA Devices Critical Jul 9, 2025

BiPAP A30 Ventilators. Intended to provide noninvasive ventilation support in adult and pediatric patients weighing more than 10 kg. BiPAP Hybrid A…

FDA Devices Critical Nov 20, 2024

Trilogy Evo Universal Ventilator. Model Number DS2000X11B. Intended for invasive and non-invasive ventilation of pediatric through adult patients we…

FDA Devices Critical Nov 20, 2024

Trilogy EV300. Model Numbers: DS2200X11B, IN2200X15B, BL2200X15B, BR2200X18B, CA2200X12B, DE2200X13B, GB2200X15B, ND2200X15B, ES2200X15B, FR2200X14B,…

FDA Devices Critical Nov 20, 2024

Aeris EVO. Model Number: VT2110X24B. Intended for invasive and non-invasive ventilation of pediatric through adult patients weighing at least 2.5 k…

FDA Devices Critical Sep 11, 2024

Trilogy Evo; Model No./Model Description -- AU2110X15B Trilogy Evo, Australia BL2110X15B Trilogy Evo, Benelux BR2110X18B Trilogy Evo, Brazil …

FDA Devices Critical Sep 11, 2024

Trilogy Evo Universal Ventilator, Model No. DS2000X11B

FDA Devices Critical May 29, 2024

BiPAP V30 Auto Ventilator, Part Number 1111178

FDA Devices Critical May 29, 2024

BiPAP A40 Ventilators: BiPAP A40, Part Numbers 1111169 (US and OUS) and (OUS ONLY)1111170 1111171 1111173 1111174 1111175 1111177 1116156…

FDA Devices Critical May 29, 2024

OmniLab Advanced + Ventilator Product Numbers 1111122 1111123 1111124 1111125 1111126 1111127 1111138 1111141 1111142 KR1111127 R1111122 R111112…

FDA Devices Critical May 29, 2024

BiPAP A30 Ventilator, Part Number 1111143 (US and OUS) OUS Only: Part Numbers 1111144 1111145 1111147 1111148 1111149 1111150 1111154 1111…

FDA Devices Critical Apr 24, 2024

Trilogy Evo Universal Ventilator, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients.

FDA Devices Critical Apr 24, 2024

LifeVentEVO2, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients. (sold outside US)

FDA Devices Critical Apr 24, 2024

Aeris EVO, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients. (sold outside US)

FDA Devices Critical Apr 24, 2024

Trilogy Evo O2, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients.

FDA Devices Critical Oct 4, 2023

Philips Respironics V60/V60 Plus Ventilator, PCBA Part Number: 453561544461 V60 Device Part Numbers 1053617 (US) and 1137276 (Philippines)

FDA Devices Critical Jun 14, 2023

Trilogy Evo O2 EV300, Model Numbers DS2200X11B, IN2200X15B, FX2200X15B, CA2200X12B, FR2200X14B, ND2200X15B, ES2200X15B, BL2200X15B, GB2200X15B, EU220…

FDA Devices Critical Jun 14, 2023

Trilogy Evo, Garbin Evo, and Aeris EVO, Model Numbers DS2110X11B, IN2110X15B, JP2110X16B, AU2110X15B, LA2110X15B, CA2110X12B, BR2110X18B, KR2110X15B,…

FDA Devices Critical Jun 14, 2023

Trilogy Evo Universal Ventilator, Model Number DS2000X11B

FDA Devices Critical Apr 12, 2023

Philips DreamStation Auto BiPAP and CPAP, Model Numbers UCDSX500S11, UDSX500S11, UDSX500S11F, UDSX700S11, UDSX700S11F, UFRX500S14. Used to deliver p…

FDA Devices Critical Jan 18, 2023

Philips Trilogy 100 Ventilator, Model Numbers 1054260, 1054096, U1054260, U1054260B, 1054260B, CA1054096B, BT1054260, 1054096B, R1054260, RSL1054260,…

FDA Devices Critical Oct 12, 2022

Wisp and Wisp Youth Nasal Mask

FDA Devices Critical Oct 12, 2022

DreamWisp Nasal Mask with Over the Nose Cushion

FDA Devices Critical Oct 12, 2022

Philips Respironics Amara View Minimal Contact Full-Face Mask

FDA Devices Critical Sep 14, 2022

Philips BiPAP A30, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insu…

FDA Devices Critical Sep 14, 2022

Philips BiPAP V30 Auto, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory…

FDA Devices Critical Sep 14, 2022

Philips OmniLab Advanced+ Intl (Flow Gen), Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (O…

FDA Devices Critical Sep 14, 2022

Philips OmniLab Advanced + with Heated Tube Humidifier, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apne…

FDA Devices Critical Feb 2, 2022

Trilogy Evo, Material Numbers DS2110X11B (USA) and KR2110X15B (Korea) The Trilogy Evo ventilator provides continuous or intermittent positive pres…

FDA Devices Critical Feb 2, 2022

Trilogy Evo Repair Kit, RP-Trilogy Evo Muffler Assembly, Material Number 1135257 The Trilogy Evo ventilator provides continuous or intermittent po…

FDA Devices Moderate Aug 25, 2021

Trilogy Evo Universal, Product number DS2000X11B

FDA Devices Moderate Aug 25, 2021

Trilogy Evo O2, Product numbers DE2100X13B, DS2100X11B, EE2100X15B, ES2100X15B, EU2100X15B, FR2100X14B, FX2100X15B, IA2100X15B, IN2100X15B, IN2100X19…

FDA Devices Moderate Aug 25, 2021

Trilogy EV300, Product numbers CA2200X12B, DS2200X11B, FX2200X15B, IN2200X15B

FDA Devices Critical Jul 21, 2021

Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent Continuous Ventilators.

FDA Devices Critical Jul 21, 2021

A-Series BiPAP A 40, A-Series BiPAP A30 Continuous Ventilator, Non-life Supporting

FDA Devices Moderate Jun 2, 2021

BiPAP A40 System Silver, JP: Continuous ventilator, non-life-supporting. Material Number: R1111177

FDA Devices Moderate Jun 2, 2021

BiPAP A30, Brazil: Continuous ventilator, non-life-supporting. Material Number: BR1111143

FDA Devices Moderate Jun 2, 2021

BiPAP A40 System Silver, JP: Continuous ventilator, non-life-supporting. Material Number: 1111177

FDA Devices Moderate Jun 2, 2021

BiPAP A40, Brazil: Continuous ventilator, non-life-supporting. Material Number: BR1111169

FDA Devices Moderate Jun 2, 2021

BiPAP A40, China: Continuous ventilator, non-life-supporting. Material Number - CN1111169

FDA Devices Critical Feb 26, 2020

Trilogy EVO Ventilator, Nordics - Model Number: ND2110X15B Trilogy Evo is intended for pediatric through adult patients weighing at least 2.5 kg. …

FDA Devices Critical Feb 26, 2020

Trilogy EVO Ventilator, France - Model Number: FR2110X14B Trilogy Evo is intended for pediatric through adult patients weighing at least 2.5 kg. T…

FDA Devices Critical Feb 26, 2020

Trilogy EVO Ventilator, EU - Model Number: EU2110X15B Trilogy Evo is intended for pediatric through adult patients weighing at least 2.5 kg. The v…

FDA Devices Critical Feb 26, 2020

Trilogy EVO Ventilator, Iberia - Model Number: ES2110X15B Trilogy Evo is intended for pediatric through adult patients weighing at least 2.5 kg. T…

FDA Devices Critical Feb 26, 2020

Garbin EVO Ventilator, Linde - Model Number: LD2110X23B Trilogy Evo is intended for pediatric through adult patients weighing at least 2.5 kg. The…

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

  • Source: FDA + CPSC + NHTSA + USDA FSIS — federal recall filings naming this firm. Verify with FDA, CPSC, NHTSA, or USDA FSIS directly.
  • Source: PlainRecalls Manufacturer Index — firm-level aggregation across all four federal recall feeds