Health product recall

Cardiomems Patient and Hospital Electronics System

Brand(s)
Last updated

Summary

Product
Cardiomems Patient and Hospital Electronics System
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

Cardiomems Patient Electronics System

All lots.

CM1100

Cardiomems Hospital Electronics System

All lots.

CM3000

Issue

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

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies

Abbott Medical

387 Technology Circle  Nw, Atlanta, Georgia, United States, 30313

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-72928

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