Medical Device Recall: Patient Information Center iX and Patient Information Center iX Expand, Software Version 4.x.
Philips North America Llc · April 19, 2024
Reason for Recall
Event Catalog information does not save when copied and transferred from one unit to another.
Distribution
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.
States Affected
NATIONWIDE
Quantity Affected
358 units (US: 45; OUS: 313)
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1827-2024
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.