Magstim recalls Rapid2 PSU Stim Interconnecting Cable due to potential high voltage cable failure. This device is used for treating major depressive disorder. Affected units may pose a risk of electrical malfunction.
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 the Rapid2 PSU Stim Interconnecting Cable because it has a potential to fail, which could lead to electrical issues. This cable is used in treating major depressive disorder. If you have this product, stop using it immediately to avoid risks.
The high voltage cable at the rear of the Rapid2 and Horizon power supply units may fail, potentially causing electrical issues. This failure could lead to malfunction or damage if the cable is used as intended.
Adult patients using this cable for major depressive disorder treatment who have the product code 3853-00 are most at risk. The recall applies to the specific cable model used with Rapid2 and Horizon power supply units.
Check for the product code 3853-00 on the Rapid2 PSU Stim Interconnecting Cable. This cable is used with Rapid2 and Horizon power supply units for treating major depressive disorder.
The Rapid2 PSU Stim Interconnecting Cable may fail and cause electrical issues. Discontinue use immediately.
Yes, this cable is indicated for the treatment of major depressive disorder in adult patients who have failed to achieve satisfactory improvement from prior antidepressant medication.
The product code is 3853-00.
The recall is due to a potential failure of the high voltage cable at the rear of the Rapid2 and Horizon power supply units.
We’ve drafted a message you can send Magstim to request your refund or repair — edit it as you like.
Subject: Recall Z-1966-2020 — Magstim Magstim Hello, I own a Magstim that is covered by recall Z-1966-2020 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.
