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The official notice did not include a photo. Check the product details and identifiers below.
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An official Health Canada notice concerns Aveir™ leadless pacemaker. 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 Published 2024-08-19.
What to do now
Contact the manufacturer if you require additional information.
Recall number
75937
Official notice
2024-08-19
The hazard
The hazard
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
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Recall Numbers
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Turn on recall alertsAffected products
Affected products
Product 1
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand: Abbott Medical, Aveir™ Leadless Pacemaker.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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