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Respironics California Recalls

53 recalls on record · September 12, 2012 to April 27, 2022 · Medical Devices

Recalls by year

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22

Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.

February 3, 2021Medical DevicesFDA
Respironics California, LLC recalls Philips Respironics V60 Ventilator Part Number 1076717 - Product Usage: intended to be used only with various combinatio
Hazard: Ventilator may experience potential issues with the backup battery failures: 1) if the battery is allowed to over discharge, or 2) if the ventilator is stored for an extended period of time without being plugged into AC power.
February 3, 2021Medical DevicesFDA
Respironics California, LLC recalls Philips Respironics V60 Ventilator Part Number 1076716 - Product Usage: intended to be used only with various combinatio
Hazard: Ventilator may experience potential issues with the backup battery failures: 1) if the battery is allowed to over discharge, or 2) if the ventilator is stored for an extended period of time without being plugged into AC power.
February 3, 2021Medical DevicesFDA
Respironics California, LLC recalls Philips Respironics V60 Ventilator Part Number R1076709 - Product Usage: intended to be used only with various combinati
Hazard: Ventilator may experience potential issues with the backup battery failures: 1) if the battery is allowed to over discharge, or 2) if the ventilator is stored for an extended period of time without being plugged into AC power.
February 3, 2021Medical DevicesFDA
Respironics California, LLC recalls Philips Respironics V60 Ventilator Part Number R1053618 - Product Usage: intended to be used only with various combinati
Hazard: Ventilator may experience potential issues with the backup battery failures: 1) if the battery is allowed to over discharge, or 2) if the ventilator is stored for an extended period of time without being plugged into AC power.
February 3, 2021Medical DevicesFDA
Respironics California, LLC recalls Philips Respironics V60 Ventilator Part Number 1076709 - Product Usage: intended to be used only with various combinatio
Hazard: Ventilator may experience potential issues with the backup battery failures: 1) if the battery is allowed to over discharge, or 2) if the ventilator is stored for an extended period of time without being plugged into AC power.
February 3, 2021Medical DevicesFDA
Respironics California, LLC recalls Philips Respironics V60 Ventilator Part Number 1053618 - Product Usage: intended to be used only with various combinatio
Hazard: Ventilator may experience potential issues with the backup battery failures: 1) if the battery is allowed to over discharge, or 2) if the ventilator is stored for an extended period of time without being plugged into AC power.
February 3, 2021Medical DevicesFDA
Respironics California, LLC recalls Philips Respironics V60 Ventilator Part Number 1053617 - Product Usage: intended to be used only with various combinatio
Hazard: Ventilator may experience potential issues with the backup battery failures: 1) if the battery is allowed to over discharge, or 2) if the ventilator is stored for an extended period of time without being plugged into AC power.
February 3, 2021Medical DevicesFDA
Respironics California, LLC recalls Philips Respironics V60 Ventilator Part Number 1053616 - Product Usage: intended to be used only with various combinatio
Hazard: Ventilator may experience potential issues with the backup battery failures: 1) if the battery is allowed to over discharge, or 2) if the ventilator is stored for an extended period of time without being plugged into AC power.
February 3, 2021Medical DevicesFDA
Respironics California, LLC recalls Philips Respironics V60 Ventilator Part Number 1053615 - Product Usage: intended to be used only with various combinatio
Hazard: Ventilator may experience potential issues with the backup battery failures: 1) if the battery is allowed to over discharge, or 2) if the ventilator is stored for an extended period of time without being plugged into AC power.
February 3, 2021Medical DevicesFDA
Respironics California, LLC recalls Philips Respironics V60 Ventilator Part Number 1053614 - Product Usage: intended to be used only with various combinatio
Hazard: Ventilator may experience potential issues with the backup battery failures: 1) if the battery is allowed to over discharge, or 2) if the ventilator is stored for an extended period of time without being plugged into AC power.
February 3, 2021Medical DevicesFDA
Respironics California, LLC recalls Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage: intended to be used only with various combinatio
Hazard: Ventilator may experience potential issues with the backup battery failures: 1) if the battery is allowed to over discharge, or 2) if the ventilator is stored for an extended period of time without being plugged into AC power.
April 8, 2020Medical DevicesFDA
Respironics California, LLC recalls Philips V60 Ventilators with Power Management PCBA part number 1055906
Hazard: Solder connection failure on Power Management printed circuit board assembly of ventilators may cause 1) Blower to lose power, spool down, and trigger visual and audible High Priority Check Vent alarm indicating a need for alternative ventilation, or 2) Intermittent connection may disrupt expected operation and trigger unexpected shutdown without alarm. Failures may lead to hypercarbia/hypoxemia
February 19, 2020Medical DevicesFDA
Respironics California, LLC recalls Respironics V680 Ventilator, Service # 850011, (OUS Only)
Hazard: Ventilator touchscreen may become frozen and fail to respond to touch commands. If a patient requires a change in therapy, there is no warning associated with an unresponsive touchcreen, and therefore the clinician would have no prior indication of a touchscreen failure and would be unable to change ventilator settings. The ventilator will continue to function at the predetermined and accepted settings required to support the patient. A delay in therapy adjustments may result in hypercarbia and/or hypoxemia.
February 19, 2020Medical DevicesFDA
Respironics California, LLC recalls Respironics RP-Touch Screen, V60/V680 Ventilator Serviced with Touchscreen RP Kit 453561511951 containing a touchscreen
Hazard: Ventilator touchscreen may become frozen and fail to respond to touch commands. If a patient requires a change in therapy, there is no warning associated with an unresponsive touchcreen, and therefore the clinician would have no prior indication of a touchscreen failure and would be unable to change ventilator settings. The ventilator will continue to function at the predetermined and accepted settings required to support the patient. A delay in therapy adjustments may result in hypercarbia and/or hypoxemia.
February 19, 2020Medical DevicesFDA
Respironics California, LLC recalls Respironics RP-UI Assy, V60 Ventilators User Interface RP-Kits, REF/P/N: 453561528931, 453561528941, 453561536451,
Hazard: Ventilator touchscreen may become frozen and fail to respond to touch commands. If a patient requires a change in therapy, there is no warning associated with an unresponsive touchcreen, and therefore the clinician would have no prior indication of a touchscreen failure and would be unable to change ventilator settings. The ventilator will continue to function at the predetermined and accepted settings required to support the patient. A delay in therapy adjustments may result in hypercarbia and/or hypoxemia.
February 19, 2020Medical DevicesFDA
Respironics California, LLC recalls Respironics V60 Ventilator, Service # 850008, REF: 1053613, 1053614, 1053617, 1053614
Hazard: Ventilator touchscreen may become frozen and fail to respond to touch commands. If a patient requires a change in therapy, there is no warning associated with an unresponsive touchscreen, and therefore the clinician would have no prior indication of a touchscreen failure and would be unable to change ventilator settings. The ventilator will continue to function at the predetermined and accepted settings required to support the patient. A delay in therapy adjustments may result in hypercarbia and/or hypoxemia.
May 24, 2017Medical DevicesFDA
Respironics California Inc recalls Philips V60 Ventilators, Material No. 850008, 1053613, 1053614, 1053615, 1053616, 1053617, 1076715, 1076716, 1076717, DU
Hazard: Over time, low-frequency vibrations can cause the pins within the female connectors on the Motor Controller to Data Acquisition Board ribbon cable to become partially displaced causing momentary high resistance that prevents or restricts data travelling through the cable during the high resistance event.
April 5, 2017Medical DevicesFDA
Respironics California Inc recalls Philips V60 Ventilator with Version 2.20 Software, Description: V 60 Ventilator,Intl Opt: CFLEX,AVAPS,PPV V60 Vent
Hazard: The V60 Ventilator with Version 2.20 software installed may falsely detect that the blower motor has stalled. If this condition occurs, the software will cause the ventilator to shut down (Vent Inop) and display Error Code 100E. Ventilatory support will cease.
December 3, 2014Medical DevicesFDA
Respironics California Inc recalls Esprit V1000 Ventilator and Esprit/V200 Conversion Ventilator The Esprit V1000 and Esprit/V200 Conversion Ventilators
Hazard: If the power supply fan mounting screws are installed incorrectly, the ends of the screws may touch the power supply printed circuit board assembly (PCBA) and short to ground. This may prevent the ventilator to switch to battery power if AC power is disrupted.
October 29, 2014Medical DevicesFDA
Respironics California Inc recalls Esprit V1000 and V200 Ventilators, Model No. V1000 and V200; and the 3rd Generation Power Supply Repair Part (RP)Kits
Hazard: A failure of a specific component may prevent the ventilators from operating on AC power or transitioning back to AC power when operating on battery. Additionally, if a battery is not present or is depleted the ventilators will not operate. This failure will cause the loss of ventilator support, which may result in hypercarbia or hypoxemia.
September 4, 2013Medical DevicesFDA
Respironics California Inc recalls Continuous Ventilator/Continuous Ventilator with Respiratory Mechanics, Model No. V1000
Hazard: The power to the Esprit Display's Backlight is interrupted, causing the GUI to flicker or go dark and making the display unreadable.
June 26, 2013Medical DevicesFDA
Respironics California Inc recalls Respironics V60 Ventilator, Model #V60 Respironics Material P/N (Philips 12 Digit P/N): 85008 (85008) 1053613 (9
Hazard: Respironics California, Inc. has initiated a recall on the V60 ventilator because of an issue with the software on the V60 Power Management Board Assembly. If a component fails on the Power Management Board Assembly, it may cause ventilator support to be lost with potentially no audible alarm from the ventilator.
September 12, 2012Medical DevicesFDA
Respironics California Inc recalls V60 Ventilator, Continuous Ventilator, Model# V60, PN 1056490 Product Usage: The V60 Ventilator is an assist Ventila
Hazard: Respironics is recalling the V60 ventilator because certain blower motor assemblies in the V60 ventilators may not meet specifications. Specifically, the impeller may not be properly seated on the blower motor shaft. This could subsequently cause the blower to cease functioning which would result in the failure of the V60 ventilator to deliver therapy to the patient due to the loss of ventilatio