The Magstim Company Limited: Medical Device Recall in 2019 - (Recall #: Z-0836-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

HORIZON Ez Arm (Part of the HORIZON TMS Therapy System.)

Product Classification:

Class II

Date Initiated: October 25, 2018

Date Posted: February 20, 2019

Recall Number: Z-0836-2019

Event ID: 81489

Reason for Recall:

A stray strand of stainless-steel cable may protrude from the heat shrink sleeving on the Balance Cable of the Ez Arm.

Status: Ongoing

Product Quantity: 27 (including 2 demos)

Code Information:

Product #: 5162-00 Serial #'s: 55308/001, 55308/002, 55310/001, 55310/002, 55446/001, 55446/002, 55447/001, 55447-002, 55631-001, 55631-002, 55631-003, 55631-004, 55632/001, 55632/002, 55632/003, 55632/004, 55841/001, 55841-002, 55841-003, 55841-004, 55842/001, 55842/002, 55842/003, 55842/004, 55843-001, PLT00015/001 and PLT00015/002

Distribution Pattern:

CA, MA, MN, PA, TX, VA, WI, and WA

Voluntary or Mandated:

Voluntary: Firm initiated