ClearanceBrief
Recall Z-0731-2024 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

Philips North America

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

DateJan 13, 2024 (initiated Nov 28, 2023)
StatusOpen, Classified
ReasonPush 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.
Root causeSoftware design
ActionOn November 28, 2023, the firm notified affected consignees through URGENT Medical Device Correction letters. This failure is applicable to Apple iOS devices only. If customers use iOS devices (e.g. iPhone, iPad, etc.) to receive event notifications: 1) Please conduct patient monitoring at the central station or patient bedside. 2) Please do not use iOS event notifications for patient monitoring. A Philips representative will contact you to schedule a visit to install a software patch to your device which will correct the current issue. Patch PIC iX 4.2.2 will be provided for PIC iX 4.X an
Quantity41 US; 773 OUS
DistributionWorldwide distribution: US (Nationwide) to states of: CA, GA, IA, MA, MI, MN, NJ, NM, NY, OH, PA, TN, TX, WA, WV; and OUS (Foreign) distribution to countries of: Australia, Austria, Belarus, Belgium, Brazil, Canada, Czech Republic, Denmark, Estonia, Faroe Islands, Finland, France, Germany, India,
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K153702M3290B Philips IntelliVue Information Center iX
Philips Medical Systems, Jun 13, 2016
K161164CareEvent inclusive of the CareEvent Mobile Application accessory
Philips Medical Systems, Jun 24, 2016