The Magstim Company Limited recalls HORIZON Ez Arm (Part of the HORIZON TMS Therapy System.)
- Recall date
- October 25, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0836-2019
- FDA classification
- Class II
- Brand / firm
- The Magstim Company Limited
- Sold / distributed
- CA, MA, MN, PA, TX, VA, WI, and WA
Why it was recalled
A stray strand of stainless-steel cable may protrude from the heat shrink sleeving on the Balance Cable of the Ez Arm.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
HORIZON Ez Arm (Part of the HORIZON TMS Therapy System.)
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