Public recall detail

Cardiac Workstation

2026-07-16

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Health products Health product recall
Quick summary

Quick summary: Cardiac Workstation. Reason: Health product recall. Category: Health products. Date: 2026-07-16.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Cardiac Workstation. Reason: Health product recall. Category: Health products. Date: 2026-07-16.

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
ProductCardiac Workstation
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82332

Affected products

ProductCardiac Workstation 5000
LotNot applicable.
Model860439
Serial numberNot applicable.
DescriptionCardiac Workstation 5000
ProductCardiac Workstation 7000
LotNot applicable.
Model860441
Serial numberNot applicable.
DescriptionCardiac Workstation 7000

Issue

The cardiac workstation can intermittently provide inaccurate data related to the patient's native heart rate. Healthcare providers were able to recognize that secondary review was needed because the patient’s clinical presentation and symptoms were not consistent with the elevated heart rate displayed by the Cardiac Workstation. Although the elevated heart rate may serve as an indicator to the clinician that the data is inaccurate, the issue also impacts the accuracy of the entire ECG report, including waveform data, measurements, and interpretive statements. This issue is related to the Wired Patient Interface Module PIM accessory used with the Cardiac Workstation. In rare cases, when the Cardiac Workstation is returned from Standby mode, the system may not set the ECG sampling rate in the Wired PIM correctly. This can cause the ECG waveform and interpretation to be inaccurate.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Cardiovascular
CompaniesPhilips Medizin Systeme Boblingen GmbhHewlett-Packard Strasse 2, Boblingen, Germany, 71034
Recall date2026-07-07
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82332
Background{}
CompaniesPhilips Medizin Systeme Boblingen GmbhHewlett-Packard Strasse 2, Boblingen, Germany, 71034
AudiencesHealthcare
Source updated2026-07-16

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

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