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

Recall Z-0731-2024 — (1) Patient Information Center iX, Model No. 866389 (2) Patient Information Center iX Expand, Model No. 866390 (3) PIC iX Hardware, Model No. 866424

U.S. FDA — Device Enforcement · United States · 2023-11-28 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0731-2024
Date of alert
2023-11-28
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: Push 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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