Aveir™ Leadless Pacemaker
Brand(s)
Last updated
Summary
Product
Aveir™ Leadless Pacemaker
Issue
Medical devices - Device compatibility
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 |
|---|---|---|
Aveir™ Leadless Pacemaker |
Not applicable. |
LSP112V |
Issue
Abbott is informing customers of the potential for Electromagnetic Interference (EMI) to cause an inadvertent mode change in a subset of Aveir™ VR LSP112V devices manufactured with firmware version 19.05.00. This issue is corrected through a firmware upgrade.
Recall start date: April 3, 2024
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies
Abbott Medical
15900 Valley View Court, Sylmar, California, United States, 91342
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-75937
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