FDANovember 15, 2018device

Xper Flex Cardio Physiomonitoring System, Software versions 1.5.16.0322 and 1.6.1.0390, Model Numbers 453564241901, 453564241911, 453564483321, 453564483331, 453564621791, 453564621801, 453564669081

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

There are 3 issues: 1) Under certain conditions, real time waveforms may not be accurately plotted or displayed. 2) The oxygen saturation (SpO2) numeric value displayed on the device may freeze. 3) In auto cycle mode, if the NIBP communication is lost, the pump would not cycle and the non-invasive blood pressure (NIBP) numeric value displayed on the device would not update.

What to do

FDA enforcement status: Terminated

Brands named

philips electronics north americaphilipsphilips electronics

UPCs

453564241901453564241911453564483321453564483331453564621791453564621801453564669081

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Xper Flex Cardio Physiomonitoring System, Software versions 1.5.16.0322 and 1.6.1.0390, Model Numbers 453564241901, 453564241911, 453564483321, 453564483331, 453564621791, 453564621801, 453564669081 — Recall Details · AllClear