Cardiomems Patient and Hospital Electronics System
Brand(s)
Last updated
Summary
Product
Cardiomems Patient and Hospital Electronics System
Issue
Medical devices - Performance issue
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: 2023-02-23
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