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FDA (Device enforcement)Recalled 2021-03-29class ii

Philips North America Llc: Philips Xper Flex Cardio (FC2010, Procedure Room and FC2020, Bedside Monitor) devices - intended for use by professional healthcare providers for complete physiologic/hemody

Is my product affected?

Philips Xper Flex Cardio (FC2010, Procedure Room and FC2020, Bedside Monitor) devices - intended for use by professional healthcare providers for complete physiologic/hemodynamic monitoring Service numbers associated with FC2010: Xper Flex Cardio 2010 Rev A 453564241901 Xper Flex Cardio 2010 Rev B 4

  • UPC 453564241901
  • UPC 00884838082113
  • UPC 453564241911
  • UPC 453564483321
  • UPC 453564483331
  • UPC 00884838083516
  • UPC 453564621791
  • UPC 00884838084902
  • UPC 453564621801
  • UPC 00884838084919
  • UPC 453564845881
  • UPC 00884838095052
  • UPC 453564675021
  • UPC 00884838103245
  • UPC 453564669081
  • UPC 00884838083820
  • UPC 453564675001
  • UPC 00884838086005
  • UPC 453564674581
  • UPC 453564845841
  • UPC 00884838093645
  • UPC 453564845861
  • UPC 00884838093652

Check against the official notice below — it lists the full affected range.

What happened

Philips North America LLC is recalling 9,208 units of its Xper Flex Cardio Physio Monitoring System (models FC2010 procedure room monitor and FC2020 bedside monitor) due to multiple performance issues. The devices, which are used by healthcare providers to monitor patient vital signs, can experience delays of up to 10 seconds in displaying ECG, invasive blood pressure, and other parameters; software crashes; failure to display oxygen saturation data; frozen displays where waveforms and numeric values stop updating; flat-line waveforms with no audible alarms; and unexpected non-physiological waveforms and heart rate values upon startup. The recall affects devices distributed nationwide and internationally, with specific lot and service numbers identified.

The source record does not specify a remedy or corrective action that affected consumers should take.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

Performance issues with the Xper Flex Cardio Physio Monitoring System include: potential delay of up to 10 seconds in displaying ECG, invasive blood pressure and other parameters; patient weight is rounded to the nearest whole kilogram;Xper IM software used with the Xper Flex Cardio Physio Monitoring System may periodically crash; No SpO2 numeric or plethysmography is displayed when SpO2 is connected o the Flex Cardio device; display of certain data from the FC2010 becomes frozen, i.e., waveforms cease sweeping and updating and the ECG, IBP, and respiration numeric values cease to update;e ECG, IBP, and respiration waveforms become flat lines and no audible alarms are produced for HR and IBP, upon start up, an unexpected non physiological ECG waveform, erratic heart rate numeric value, and non-physiological display of any other active waveforms may appear on the Boom Monitor

Details from the source

Reason for recall: Performance issues with the Xper Flex Cardio Physio Monitoring System include: potential delay of up to 10 seconds in displaying ECG, invasive blood pressure and other parameters; patient weight is rounded to the nearest whole kilogram;Xper IM software used with the Xper Flex Cardio Physio Monitoring System may periodically crash; No SpO2 numeric or plethysmography is displayed when SpO2 is connected o the Flex Cardio device; display of certain data from the FC2010 becomes frozen, i.e., waveforms cease sweeping and updating and the ECG, IBP, and respiration numeric values cease to update;e ECG, IBP, and respiration waveforms become flat lines and no audible alarms are produced for HR and IBP, upon start up, an unexpected non physiological ECG waveform, erratic heart rate numeric value, and non-physiological display of any other active waveforms may appear on the Boom Monitor Distribution: Nationwide Foreign: Argentina Australia Austria Bangladesh Belgium Bulgaria Canada Chile China Croatia Cyprus Czech Republic Denmark Dominican Republic Ecuador Egypt Estonia Finland France Germany Greece Hungary Iceland India Indonesia Iran Iraq Ireland Israel Italy Jordan Kazakhstan Kenya Korea, Republic of Kuwait Latvia Lebanon Libya Lithuania Malaysia Mauritius Mexico Mongolia Morocco Myanmar N Quantity: 9208 units WW Lot/code info: Service Number/ UDI # 453564241901 (01)00884838082113; 453564241911 (01)00884838082113; 453564483321 (01)00884838082113; 453564483331 (01)00884838083516; 453564621791 (01)00884838084902; 453564621801 (01)00884838084919; 453564845881 (01)00884838095052; 453564675021 (01)00884838103245; 453564669081 (01)00884838083820; 453564675001 (01)00884838086005; 453564674581 (01)00884838083820; 453564845841 (01)00884838093645; 453564845861 (01)00884838093652

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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