medical Class II Updated 2024-01-24

Philips North America recalls (1) Patient Information Center iX, Model No. 866389 (2) Pat

Recalled Product

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


Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI: (1) 00884838104594 (2) 00884838112070 (3) 00884838121782 Software: PIC iX Version 4.X
View official government recall

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