Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35
FDA Recall #Z-2192-2025 — Class II — March 21, 2025
Product Description
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.
Recalling Firm
Phasor Health, LLC — Houston, TX
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Devices
Product Quantity
1,064
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
Code Information
UDI-DI: B775270S0, B775320L0, B7754500, B7755300, B7756350. Lot: 241002450, 241002530, 241009450, 241009530, 241016450, 241016530, 241023450, 241023530, 241030450, 241030530, 24112027S, 24121827S, 24122727S, 25012227S, 24082832L, 24102332L, 241227450, 241220635, 250122635, 241227530, 250122530.
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated