Health product recall

LINQ II Insertable Cardiac Monitor (ICM)

Brand(s)
Last updated

Summary

Product
LINQ II Insertable Cardiac Monitor (ICM)
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
LINQ II Insertable Cardiac Monitor (ICM) More than 10 numbers, contact manufacturer. LNQ22

Issue

Medtronic is notifying customers of a population of LINQ II Insertable Cardiac Monitors (ICM) that underwent a manufacturing process that may allow for moisture to impact electrode performance. This may create the potential for amplified noise and/or overall signal reduction of the ICM, which may interfere with intended recordings of heart rhythms.

Recall start date: November 2, 2023

Additional information

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

Medtronic Inc.

710 Medtronic Parkway N.E., Minneapolis, Minnesota, United States, 55432

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-74622