Phasor Health, LLC recalls Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35

Recall date

March 21, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2192-2025

FDA classification

Class II

Brand / firm

Phasor Health, LLC

Sold / distributed

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

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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