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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 8 of 8 Results
510(K) Number: K153702
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Patient Information Center iX; Software Version Number: 4.5.0 2 01/22/2026 FEI # 3006648320
Philips North America
DIVA 24 Inch Widescreen LCD Touch Display - Used with the Philips PIC iX system central monitoring ... 2 09/30/2024 FEI # 3016618143
Philips North America Llc
Patient Information Center iX and Patient Information Center iX Expand, Software Version 4.x. 2 05/15/2024 FEI # 3016618143
Philips North America Llc
Philips Patient Information Center (PIC) iX Uninterruptable Power Supply (UPS): 1. APC (Schneider E... 2 04/25/2024 FEI # 3016618143
Philips North America Llc
Patient Information Center iX (PIC iX), Model Numbers 866389, 866390 (PIC iX Expand), and 866424 (PI... 2 03/27/2024 FEI # 3006648320
Philips North America
(1) CareEvent, Model No. 866435 (2) CareEvent Upgrade, Model no. 866436 2 01/13/2024 FEI # 3006648320
Philips North America
Patient Information Center iX with Software Version Number 4.x in the following: (1) Patient Info... 2 09/19/2023 FEI # 3016618143
Philips North America Llc
Philips Patient Information Center iX configured with a regional setting which uses a comma for a de... 3 06/12/2019 FEI # 1218950
Philips North America, LLC
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