Public recall detail

Patient Information Centre iX

2026-08-20

medium
Health products Health product recall
Quick summary

Quick summary: Patient Information Centre iX. Reason: Health product recall. Category: Health products. Date: 2026-08-20.

Recommended action

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.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandPhilips Medizin Systeme Boblingen Gmbh
ProductPatient Information Centre iX
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82511

Affected products

ProductPatient Information Centre iX
LotNot applicable.
ModelVERSION 4.2
Serial numberNot applicable.
DescriptionPatient Information Centre iX
ProductPatient Information Centre iX
LotNot applicable.
ModelVERSION 4.0
Serial numberNot applicable.
DescriptionPatient Information Centre iX
ProductPatient Information Centre iX
LotNot applicable.
Model4.5
Serial numberNot applicable.
DescriptionPatient Information Centre iX
ProductPatient Information Centre iX
LotNot applicable.
ModelVERSION 4.3
Serial numberNot applicable.
DescriptionPatient Information Centre iX
ProductPatient Information Centre iX
LotNot applicable.
Model4.4
Serial numberNot applicable.
DescriptionPatient Information Centre iX
ProductPatient Information Centre iX
LotNot applicable.
ModelVERSION 4.1
Serial numberNot applicable.
DescriptionPatient Information Centre iX

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
AudienceHealthcare
CategoryHealth products - Medical devices - General hospital and personal use
CompaniesPhilips Medizin Systeme Boblingen GmbH Hewlett-Packard Strasse 2, Boblingen, Germany, 71034
Recall date2026-08-12
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82511
Background{}
CompaniesPhilips Medizin Systeme Boblingen GmbH Hewlett-Packard Strasse 2, Boblingen, Germany, 71034
AudiencesHealthcare
Source updated2026-08-20

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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