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Health Canada Medical devices

Aveir™ Leadless Pacemaker

Issued August 19, 2024
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
Hazard description
Device compatibility
Product
Product name
Aveir™ Leadless Pacemaker
Reference
ID
RA-75937