FDA recall: Brand Name: HeartMate

The FDA has classified an open recall of Thoratec's HeartMate 3 Mobile Power Unit (model 107754) due to a manufacturing defect in the power cord's V-Lock feature. The misalignment prevents the locking mechanism from securing properly, creating a risk of accidental disconnection from the power unit. For PT professionals treating patients with left ventricular assist devices, awareness of this recall is important when working with patients dependent on this cardiac support equipment.

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