HeartMate recalls Mobile Power Unit AC Power Cord model 107760 due to misaligned V-Lock feature causing unintended disconnect. Affected patients should check if their device uses this model.
Due to misaligned V-Lock feature on the Mobile Power Unit power cords, which prevents the locking mechanism from properly engaging with the Mobile Power Unit and may cause unintended disconnect.
HeartMate is recalling its Mobile Power Unit AC Power Cord model 107760 because the V-Lock feature may not lock properly, causing the cord to disconnect unexpectedly. This could lead to the device losing power during critical medical use, potentially causing harm to patients with heart failure.
The V-Lock feature on the AC power cord may not engage properly with the Mobile Power Unit, causing the cord to disconnect unexpectedly. This could lead to the device losing power during critical medical use, which might be harmful for patients with heart failure who rely on continuous support.
Patients using the HeartMate 3" Left Ventricular Assist System (LVAS) with the Mobile Power Unit AC Power Cord model 107760 are affected. Those with the device in active use are most at risk due to potential power loss during critical medical functions.
Check for the model number 107760 on the AC Power Cord label. The Mobile Power Unit is part of the HeartMate 3" Left Ventricular Assist System (LVAS) used for patients with advanced heart failure.
Look for the model number 107760 on the AC Power Cord label to confirm if it is affected.
If the cord is affected, make sure the V-Lock engages fully before using the device to prevent unintended disconnects.
The V-Lock feature on the AC Power Cord model 107760 may not engage properly with the Mobile Power Unit, causing unintended disconnects that could lead to power loss during critical medical use.
No, this recall specifically affects the Mobile Power Unit AC Power Cord model 107760 used with the HeartMate 3" Left Ventricular Assist System (LVAS).
Check the model number on the cord. If it is model 107760, ensure the V-Lock engages fully before use to prevent unintended disconnects.
We’ve drafted a message you can send HeartMate to request your refund or repair — edit it as you like.
Subject: Recall Z-2290-2025 — HeartMate HeartMate Hello, I own a HeartMate that is covered by recall Z-2290-2025 from HeartMate. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
