Class II

Medical Device Recall: Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35

Phasor Health, LLC · March 21, 2025

Reason for Recall

Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time.

Distribution

US: PA, IN, AZ, MO, LA, FL, TX, MA, OH, TN, MI, WV, VA, CA, DE, NH, GA, SC, GU, NY, NJ, MN, WI, NE, WA, IL, AR, PR, VT

States Affected

AR, AZ, CA, DE, FL, GA, IL, IN, LA, MA, MI, MN, MO, NE, NH, NJ, NY, OH, PA, SC, TN, TX, VA, VT, WA, WI, WV

Quantity Affected

1,064

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2192-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Phasor Health, LLC Medical Device Recall: Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35 | SafeCheck