Phasor Health, LLC is recalling 1,064 Phasor Drills used in neurosurgical procedures because the batteries may be installed in the wrong direction. This defect can prevent the drill from operating correctly, which can lead to delays during surgery while staff troubleshoot the equipment. No injuries or incidents have been reported in connection with this issue.
If the battery is oriented incorrectly, the drill may fail to power on or lose power during a neurosurgical procedure. This delay could increase the time a patient is under anesthesia and interrupt critical surgical steps.
Quantity affected: 1,064 units.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
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Sources: FDA iRES · Raw API Response
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