Quick summary: Patient Information Centre iX. Reason: Health product recall. Category: Health products. Date: 2026-08-20.
Patient Information Centre iX
2026-08-20
Recommended action: compare your product with the official notice and follow the instructions published by the official source.
Recall details
Quick summary: Patient Information Centre iX. Reason: Health product recall. Category: Health products. Date: 2026-08-20.
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
Affected products
Issue
Philips received reports that some PIC iX systems were frozen and could not be used. It was determined that failure of the watchdog may cause the system to be in an unknown state and therefore potentially prevent alarms from being generated or logged. Following the initial system error which triggers the watchdog, staff may observe unexpected system behavior while the watchdog attempts recovery. The observed behavior depends on the underlying software issue and may include:-Inability to interact with the PIC iX user interface. If real-time waveforms, numeric data,and alarms remain operational, there is no impact to bedside or central monitoring and alarming.-The user will not recognize the device issue before the hazardous situation occurs if theobserved behavior is: Loss of central alarming, Loss of, or frozen, waveforms/data display-Bedside monitors and telemetry devices could generate a "No Central Mon" INOP
What you should do
- Contact the manufacturer if you require additional information.
Additional official information
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
Frequently asked questions
Answers based on the official recall notice.
Product images
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