Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0035-2025 — Patient Information Center iX, Product Code 866386, and Patient Information Center iX Expand, Product Code 866390, Software Revision 4.0.1

U.S. FDA — Device Enforcement · United States · 2023-04-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0035-2025
Date of alert
2023-04-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Philips North America
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00884838104594
Reported risk: During extended operation of the MX40 with the PIC iX, the DHCP (Dynamic Host Configuration Protocol) lease can expire on the MX40. If the DHCP lease expires while the device is offline, upon reconnecting with the PIC iX, a new IP address will be assigned to the MX40. The PIC iX will not recognize the new IP address after reconnecting and therefore the expecting settings sync fails.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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