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Cardiomems patient and hospital electronics system
Official notice
23 Feb 2023
Last checked
23 Feb 2023
An official Health Canada notice concerns Cardiomems patient and hospital electronics system. Abbott has identified that when the Cardiomems Patient Electronics Systems (model CM1100) and Cardiomems Hospital Electronics Systems (HES) (model CM3000) are used to take a reading with the pulmonary artery (pa) sensor, the radiofrequency (RF) emissions at certain frequencies are higher than levels listed in the instructions for use (IFU). Recall start date: February 7, 2023 Published 2023-02-23.
What to do now
Contact the manufacturer if you require additional information.
Recall number
72928
Official notice
2023-02-23
The hazard
The hazard
Abbott has identified that when the Cardiomems Patient Electronics Systems (model CM1100) and Cardiomems Hospital Electronics Systems (HES) (model CM3000) are used to take a reading with the pulmonary artery (pa) sensor, the radiofrequency (RF) emissions at certain frequencies are higher than levels listed in the instructions for use (IFU). Recall start date: February 7, 2023
How to check if you're affected
How to check if you're affected
Compare the VIN on your vehicle against the official list. If your VIN is listed, follow the official notice.
Recall Numbers
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Affected products
Product 1
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Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected vehicles were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand
Manufacturer
Phone
Brand: Abbott Medical, Cardiomems Patient And Hospital Electronics System.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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