Magstim recalls Horizon PSU Stim Interconnecting Cable due to potential high voltage cable failure. This could pose a risk of serious injury during use for major depressive disorder treatment.
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.
Magstim is recalling Horizon PSU Stim Interconnecting Cables because the high voltage cable at the rear of the power supply unit might fail. This could lead to serious injury during use for treating major depressive disorder in adults.
The high voltage cable at the rear of the power supply unit may fail, potentially causing serious injury during use. This failure could occur when the cable is under stress or during normal operation for treating major depressive disorder.
Adult patients using Horizon for major depressive disorder treatment who have the specific product model. Patients who have received the product after the indicated date are most at risk.
Check for the product model number 5188-00 on the Horizon PSU Stim Interconnecting Cable. The product is intended for treating major depressive disorder in adults who have not responded to prior antidepressant medication.
Look for the product model number 518: 5188-00 on the Horizon PSU Stim Interconnecting Cable.
The recall indicates a potential for high voltage cable failure, so it is not safe to use without the remedy.
The recall does not specify a remedy, so contact Magstim directly for guidance.
Adult patients using Horizon for major depressive disorder treatment who have the specific product model are most at risk.
We’ve drafted a message you can send Magstim to request your refund or repair — edit it as you like.
Subject: Recall Z-1965-2020 — Magstim Magstim Hello, I own a Magstim that is covered by recall Z-1965-2020 from Magstim. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
