LINQ II Insertable Cardiac Monitor (ICM)
Brand(s)
Last updated
Summary
Product
LINQ II Insertable Cardiac Monitor (ICM)
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 |
|---|---|---|
| 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
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