FDA recall Z-2192-2025

Phasor Health, LLC · Class II · device

Product

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

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

Key facts

Status
Ongoing
Initiation date
2025-03-21
Report date
2025-08-06
Voluntary/Mandated
Voluntary: Firm initiated
Location
Houston, TX, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2192-2025