Magstim recalls HORIZON Ez Arm devices with specific serial numbers due to potential stray stainless-steel cable protrusion from heat shrink sleeving.
A stray strand of stainless-steel cable may protrude from the heat shrink sleeving on the Balance Cable of the Ez Arm.
Magstim is recalling specific models of the HORIZON Ez Arm device because a stray stainless-steel cable may protrude from the heat shrink sleeving. This could cause injury if the cable moves and contacts the patient during treatment.
A stray strand of stainless-steel cable may protrude from the heat shrink sleeving on the Balance Cable. If this cable moves during treatment, it could contact the patient and cause injury.
Patients receiving transcranial magnetic stimulation (TMS) therapy using the recalled HORIZON Ez Arm devices are most at risk. The affected units have specific serial numbers listed in the recall notice.
Check your HORIZON Ez Arm device for the specific serial numbers listed: 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.
Identify your HORIZON Ez Arm device's serial number to see if it matches the listed numbers in the recall.
The HORIZON Ez Arm is part of the HORIZON TMS Therapy System used for transcranial magnetic stimulation treatments.
The affected serial numbers are: 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.
The recall record does not mention any remedy or fix for this issue.
We’ve drafted a message you can send Magstim to request your refund or repair — edit it as you like.
Subject: Recall Z-0836-2019 — Magstim Magstim Hello, I own a Magstim that is covered by recall Z-0836-2019 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.
