Quick summary
Quick summary: Philips Breast Coils. Date: 2025-01-30.
Public recall detail
Philips Breast Coils
2025-01-30
Recall
Safety notice
Recommended action
Recommended action: compare your product with the official notice and follow the instructions published by the official source.
Recall details
Quick summary: Philips Breast Coils. Date: 2025-01-30.
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
ProductIntelliVue MX Patient Monitor System-IntelliBridge Module EC10
IssueMedical devices - Performance
Recall classType II
IdentificationRA-76881
Affected products
ProductIntelliVue MX Patient Monitor System-IntelliBridge Module EC10
LotNot applicable.
Model865115
Serial numberNot applicable.
DescriptionIntelliVue MX Patient Monitor System-IntelliBridge Module EC10
Issue
Potential safety issue concerning IntelliVue Patient Monitor (host monitor) with IntelliBridge EC10 Module and EC5 ID-Module interfacing with the Hamilton ventilator failing to alarm for "No Device Data" INOP.
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 Gmbh Hewlett-Packard Strasse 2, Boblingen, Germany, 71034
Recall date2025-01-21
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-76881
Background{}
CompaniesPhilips Medizin Systeme Boblingen Gmbh Hewlett-Packard Strasse 2, Boblingen, Germany, 71034
AudiencesHealthcare
Source updated2026-03-11
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
FAQ
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Product images
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