Lutronic Corporation: Medical Device Recall in 2025 - (Recall #: Z-0146-2026)

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:

XERF EFFECTOR 60. Electrosurgical unit.

Product Classification:

Class II

Date Initiated: September 4, 2025

Date Posted: October 22, 2025

Recall Number: Z-0146-2026

Event ID: 97620

Reason for Recall:

Manufacturing defects in devices manufactured from 4/1/25 to 8/20/25 can on rare occasions result in adverse events for patients.

Status: Ongoing

Product Quantity: 7,490 units

Code Information:

Model/Catalog Number: 1101210000, 1101210100, 1101210200; UDI: 08809447657752, SERIAL/LOT: MP60J25C02, MP60J25G05, MP60J25G06, MP60J25H03, and MP60J25H01. Devices manufactured from 04/01/25 to 08/20/25.

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of CA, IL, MA, NJ, NY, PA, TX, and UT. The countries of Canada, South Korea, Hong Kong, Japan, Singapore, Vietnam, Myanmar, Philippines, Taiwan, and Thailand.

Voluntary or Mandated:

Voluntary: Firm initiated