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Heartmate 3™ system controller

Official notice

17 Oct 2025

HighHealth Canada

An official Health Canada notice concerns Heartmate 3™ system controller. Abbott is initiating a voluntary medical device recall for the HeartMate II® and HeartMate 3™ System Controllers. This recall does not involve device removal from where they are used or sold. Abbott has observed an increase in customer complaints about the controller Backup Battery Fault Alarm. This alarm is indicated by a flashing yellow wrench on the user interface of the System Controllers. When the controller is connected to an external power source (e.g. 14V batteries or AC power via the Mobile Power Unit), this is an advisory alarm and does not indicate a critical system failure or impact pump functionality. To reduce future instances of the Backup Battery Fault Alarm, Abbott is advising that when performing backup battery installation or replacement, clinicians should minimize excessive handling, movement, stress and pulling at the interface between the ribbon cable and controller. An example of excessive handling would be using the ribbon cable to hold the weight of the controller. Please remind patients and caregivers to follow the patient handbook: if System Controller Backup Battery Fault Alarm is active, patients should first ensure that no other alarms are active, and then they should call their hospital contact as soon as possible for diagnosis and instructions. Patients and caregivers should not immediately attempt to exchange the system controller without clinical guidance. Published 2025-10-17.

What to do now

Contact the manufacturer if you require additional information.

Recall number

78313

Official notice

2025-10-17

The hazard

Abbott is initiating a voluntary medical device recall for the HeartMate II® and HeartMate 3™ System Controllers. This recall does not involve device removal from where they are used or sold. Abbott has observed an increase in customer complaints about the controller Backup Battery Fault Alarm. This alarm is indicated by a flashing yellow wrench on the user interface of the System Controllers. When the controller is connected to an external power source (e.g. 14V batteries or AC power via the Mobile Power Unit), this is an advisory alarm and does not indicate a critical system failure or impact pump functionality. To reduce future instances of the Backup Battery Fault Alarm, Abbott is advising that when performing backup battery installation or replacement, clinicians should minimize excessive handling, movement, stress and pulling at the interface between the ribbon cable and controller. An example of excessive handling would be using the ribbon cable to hold the weight of the controller. Please remind patients and caregivers to follow the patient handbook: if System Controller Backup Battery Fault Alarm is active, patients should first ensure that no other alarms are active, and then they should call their hospital contact as soon as possible for diagnosis and instructions. Patients and caregivers should not immediately attempt to exchange the system controller without clinical guidance.

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

78313

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Affected products

Product 1

Affected products - HeartMate 3™ System Controller, Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 106531US

Product 2

Affected products - HeartMate 3™ System Controller Low Flow 2.0, Lot or serial number - s/n: HSC-138822, Model or catalogue number - 106531LF2

Product 3

Affected products - HeartMate 3™ System Controller Low Flow 2.0, Lot or serial number - s/n: HSC-122360, Model or catalogue number - 106531LF2

Product 4

Affected products - HeartMate 3™ LVAS Implant Kit, Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 106524US

Risk / hazard

Abbott is initiating a voluntary medical device recall for the HeartMate II® and HeartMate 3™ System Controllers. This recall does not involve device removal from where they are used or sold. Abbott has observed an increase in customer complaints about the controller Backup Battery Fault Alarm. This alarm is indicated by a flashing yellow wrench on the user interface of the System Controllers. When the controller is connected to an external power source (e.g. 14V batteries or AC power via the Mobile Power Unit), this is an advisory alarm and does not indicate a critical system failure or impact pump functionality. To reduce future instances of the Backup Battery Fault Alarm, Abbott is advising that when performing backup battery installation or replacement, clinicians should minimize excessive handling, movement, stress and pulling at the interface between the ribbon cable and controller. An example of excessive handling would be using the ribbon cable to hold the weight of the controller. Please remind patients and caregivers to follow the patient handbook: if System Controller Backup Battery Fault Alarm is active, patients should first ensure that no other alarms are active, and then they should call their hospital contact as soon as possible for diagnosis and instructions. Patients and caregivers should not immediately attempt to exchange the system controller without clinical guidance.

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Abbott Medical, Heartmate 3™ System Controller.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type I

App estimate

high

Recall details

Recall number

78313

Classification

Type I

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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