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Philips North America Llc recalls Patient Information Center iX and Patient Information Center iX Expand, Software Version 4.x.
Recalled May 22, 2024 · FDA recall Z-1827-2024 · Philips North America
Hazard
Event Catalog information does not save when copied and transferred from one unit to another. · FDA Class II
Units
358 units (US: 45; OUS: 313)
Sold at
Worldwide - US Nationwide distribution in the states of CA, FL, GA, IA, MA, MI, MN, MO, NJ, NM, NY, OH, PA, TN, TX, WA, WV, & DC. The countries of AE, AT, AU, BE, BR, CA, CH, CZ, DE, DK, ES, FI, FR, GB, IE, IL, IN, IT, JP, KR, LT, NL, NO, OM, PL, PT, RO, SE, SG, SK, TH, & ZA.
Description
Event Catalog information does not save when copied and transferred from one unit to another.
Product
Patient Information Center iX and Patient Information Center iX Expand, Software Version 4.x.
Manufacturer(s)
Philips North America Llc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →