Every recall we track for Philips Respironics, Inc. — 93 in all — plus the complaints and injury reports the public filed about them.
Philips Respironics recalls Trilogy Evo ventilators with software version 1.05.15.00 due to potential tidal volume discrepancies when used with non-pneumatic nebulizers. Affected units may not deliver correct breathing support.
Philips Respironics recalls Trilogy Evo ventilators with software version 1.05.15.00 due to potential obstruction alarm failure. Affected users should contact Philips for updates.
Philips Respironics recalls Trilogy EV300 ventilators with software version 1.05.15.00 due to potential failure of obstruction alarms, which may not trigger within standard timeframes.
Philips Respironics recalls Trilogy Evo Universal ventilators with software version 1.05.15.00 due to potential failure of the obstruction alarm, which may not trigger within standard timeframes.
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 Respironics recalls Trilogy Evo O2 ventilators with software version 1.05.15.00 due to potential tidal volume discrepancies when using non-pneumatic nebulizers. Affected units may not deliver correct oxygen levels.
Philips Respironics recalls Trilogy EV300 ventilators with software version 1.05.15.00 due to potential tidal volume discrepancies when using non-pneumatic nebulizers. Affected users should contact Philips for guidance.
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 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 Respironics recalls DreamStation Auto CPAP devices with a programming error that may cause incorrect device configuration. Affected units include specific model numbers and serials. Consumers should contact Philips for guidance.
Philips Respironics recalls DreamStation Auto Non-Continuous Ventilators with a programming error that may cause incorrect device configuration. Affected units have specific model and serial numbers listed in the recall notice.
Philips Respironics recalls DreamStation Auto BiPAP non-continuous ventilators with a programming error that could cause incorrect device configuration. Affected models include UDSX70:11F and specific serial numbers. Contact for remedy.
Philips Respironics
Philips Respironics
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 Respironics recalls Trilogy Evo O2 ventilators with specific model numbers due to potential aerosol buildup causing inaccurate flow measurements. Affected units may need adjustment to prevent incorrect readings.
Philips Respironics recalls LifeVent EVO2 ventilators (model SP2100X26B) due to potential aerosol buildup causing inaccurate flow readings. Affected units may require correction to avoid incorrect ventilation settings.
Philips Respironics recalls Garbin Evo ventilators (model LD2110X23B) due to potential inaccurate flow measurements from aerosol deposits. Affected units may require cleaning or adjustment to ensure proper ventilation.
Philips Respironics recalls Aeris EVO ventilators (model VT2110X24B) due to potential inaccurate flow measurements from aerosol deposits. Affected units sold to patients weighing at least 2.5 kg in institutional or home settings.
Philips Respironics recalls Trilogy EV300 ventilators with specific model numbers due to potential aerosol buildup causing inaccurate flow measurements. Affected users should check their model numbers and contact Philips for details.
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 Respironics recalls Trilogy Evo EV300 ventilators with specific model numbers for software safety updates to prevent potential issues. Affected units include various international models with unique serial numbers.
Philips Respironics recalls specific Trilogy Evo Universal Ventilator models (DS2000X11B) due to software safety issues. Users must install update version 1.05.10.00 or the user manual addendum to resolve identified risks.
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 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 Respironics recalls BiPAP A30 Ventilators with specific part numbers (US and OUS) due to potential interruption of therapy, which may lead to hypoventilation, hypoxemia, hypercarbia, respiratory failure, or death in vulnerable patients.
Philips Respironics recalls BiPAP A40 Ventilators with specific part numbers due to potential interruption of therapy during ventilator inoperative alarms, which may lead to hypoventilation, hypoxemia, hypercarbia, or respiratory failure in vulnerable patients.
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 Respironics recalls Trilogy Evo ventilators (all software versions except 1.05.06.00) due to potential sudden loss of ventilation when battery or power alarms trigger without actual power loss.
Philips Respironics recalls Garbin EVO ventilators (all software versions except 1.05.06.00) sold outside the US due to potential sudden loss of ventilation from battery or power alarms when unit has sufficient power.
Philips Respironics recalls all Trilogy EV300 ventilators except software version 1.05.06.00 due to potential sudden loss of ventilation when battery or power alarms trigger while unit has sufficient power.
Philips Respironics recalls Trilogy Evo O2 ventilators (all software versions except 1.05.06.00) due to potential sudden loss of ventilation when battery alarm triggers but power is still sufficient. Affected units have specific model numbers and serials listed in the recall.
Philips Respironics recalls Aeris EVO ventilators (all software versions except 1.05.06.00) sold outside US due to potential sudden loss of ventilation when battery alarm triggers but unit has power.
Philips Respironics recalls LifeVentEVO2 ventilators (all software versions except 1.05.06.00) sold outside the US due to potential sudden loss of ventilation when battery is depleted or power is lost.
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 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 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 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 Respironics recalls Trilogy Evo O2 and LifeVent EVO2 models with serial numbers starting with H236054270DD5. Environmental debris can accumulate on the internal flow sensor, potentially causing inaccurate pressure delivery and patient harm if not addressed by a care provider.
Philips Respironics recalls Trilogy Evo Universal Ventilators (Model DS2000X11B) for potential safety issues in pediatric patients. Affected units have specific serial numbers; users should stop using and contact Philips for details.
Philips Respironics recalls Trilogy Evo, Garbin Evo, and Aeris EVO models with specific serial numbers due to potential environmental debris accumulation causing inaccurate pressure delivery, which could lead to patient harm if not addressed by a care provider.
Philips Respironics is a leading manufacturer of medical devices, including ventilators, monitors, and other respiratory care products.
Philips Respironics recalls Trilogy Evo O2 and LifeVentEVO2 portable ventilators with model numbers DS2100X11B, IN2100X15B, IN2100X19, etc. for inaccurate oxygen delivery that may lead to under-delivery of oxygen during high concentration therapy.
Philips Respironics recalls Trilogy Evo Universal Portable Electric Ventilators (Model DS2000X11B) due to potential oxygen delivery inaccuracies below required tolerance, which may lead to under-delivery of oxygen during high concentration therapy.
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 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.
Philips recalls some Garbin Ventilators (model 1058180B) where silicone foam may separate and block air inlet, reducing therapy volume or causing alarms. Affected units have specific serial numbers.
Philips recalls Trilogy 200 Ventilators with specific model numbers due to potential separation of silicone sound abatement foam, which could block air intake and reduce therapy effectiveness.
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 Respironics recalls DreamWear Full Face Masks due to no known magnetic risks for patients with implantable devices or metallic splinters in eyes. All units with specific model numbers are affected.
Philips Respironics recalls Therapy Mask 3100 NC/SP models due to potential magnetic components not affecting patients with implantable devices or metallic eye splinters.
Philips Respironics recalls Amara View Minimal Contact Full-Face CPAP masks due to no known magnetic risks for patients with implantable devices or metallic splinters in eyes. No action required.
Philips Respironics recalls DreamWisp Nasal Mask with Over the Nose Cushion due to no known magnetic component risks for patients with implantable devices or metallic eye splinters.
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 recalls OmniLab Advanced+ CPAP machines due to plastic parts causing VOC off-gassing. Affected units have specific serial numbers. Stop using immediately to avoid potential health risks.
Philips Respironics recalls BiPAP A40 (Rx Only) devices with nonconforming plastic that may off-gas VOCs. Affected units have specific model and serial numbers. Consumers should stop using and contact Philips for replacement.
Philips recalls OmniLab Advanced + with Heated Tube Humidifier (Rx Only) due to potential VOC off-gassing from nonconforming plastic. Affected units have specific UDI-DI and model numbers. Consumers should contact Philips for details.
Philips recalls specific models of OmniLab Advanced+ Intl (Flow Gen) ventilators due to plastic components off-gassing VOCs. Affected units may pose health risks; contact Philips for details.
Philips recalls BiPAP V30 Auto devices with nonconforming plastic that may off-gas VOCs. Affected units have specific model and serial numbers. Contact Philips for details.
