Home / Recalls / Medical Devices
Phasor Health, LLC recalls Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35
Recalled August 6, 2025 · FDA recall Z-2192-2025 · Phasor Health
Hazard
Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time. · FDA Class II
Units
1,064
Sold at
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
Description
Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time.
Product
Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35
Manufacturer(s)
Phasor Health, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →