Class 2 Device Recall Horizon; The Rapid

• Date Initiated by Firm: March 23, 2020
• Create Date: May 13, 2020
• Recall Status: Terminated on September 20, 2024
• Recall Number: Z-1965-2020
• Recall Event ID: 85393
• 510(K)Number: K051864 K143531 K162935 K180907 K182853 K183376
• Product Classification: Transcranial magnetic stimulator - Product Code OBP
• Product: Horizon PSU Stim Interconnecting Cable - Product Usage: Horizon is indicated for the treatment of Major Depressive Disorder in adult patients who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode.
• Code Information: Product Number: 5188-00
• Recalling Firm/ Manufacturer: The Magstim Company Limited; Spring Gardens; Whitland United Kingdom
• For Additional Information Contact: Tom Campbell; 612-2255868
• Manufacturer Reason for Recall: It was identified that there is a potential for the Stim Interconnecting high Voltage Cable located at the rear of the Rapid2 and Horizon power supply unit to fail.
• FDA Determined Cause: Nonconforming Material/Component
• Action: The Magstim Company Ltd notified customers on about 3/23/2020 via URGENT FIELD SAFETY NOTICE Medical Device Recall letter. The letter instructed customers to identify all affected products at their facility, raise awareness to all those who need to be aware within their organization, notify customers if the product was further distributed, and complete and return the provided acknowledgement form, so Magstim Company can contact them to arrange replacement of the cable. Once customers have returned the acknowledgement form, Magstim Company will arrange for a new cable to be sent to you or your technical personnel. This will be accompanied by instructions on how to install the new cable. Magstim Technical Service Team can guide you through the installation via telephone or video call. This to limit transmission during the current pandemic COVID-19.
• Quantity in Commerce: 71 units total
• Distribution: Worldwide distribution - US Nationwide distribution including in the states of AL, AR, CA, CT, TN, IL, MN, MT, NC, NJ, NY, PA, SC, TX, WA, and the countries of Cyprus, China, Iran, Saudi Arabia, UK, Italy, Malaysia, Spain, Taiwan, Vietnam, Australia, Japan, Turkey, France and Israel.
• Total Product Life Cycle: TPLC Device Report

¹ A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
² Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
³ For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.

• 510(K) Database: 510(K)s with Product Code = OBP; 510(K)s with Product Code = OBP; 510(K)s with Product Code = OBP