Phasor Health, LLC: Medical Device Recall in 2025 - (Recall #: Z-2192-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: March 21, 2025

Date Posted: August 6, 2025

Recall Number: Z-2192-2025

Event ID: 97089

Reason for Recall:

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

Status: Ongoing

Product Quantity: 1,064

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.

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated