FDANovember 28, 2023device

(1) Patient Information Center iX, Model No. 866389 (2) Patient Information Center iX Expand, Model No. 866390 (3) PIC iX Hardware, Model No. 866424

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

The hazard

Push notifications may fail to send to the user under certain conditions. This could potentially result in patient harm due to delay in detection of a change in patient condition.

What to do

FDA enforcement status: Ongoing

Brands named

philips north americaphilipsphilips north

UPCs

008848381045940088483811207000884838121782

Recall history

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

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