Reported Feb 20, 2019 · Ongoing

HORIZON Ez Arm (Part of the HORIZON TMS Therapy System.)

The Magstim Company Limited

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: The Magstim Company Limited · Spring Gardens · Whitland, N/A · N/A

Is this the product you have?

  • HORIZON Ez Arm (Part of the HORIZON TMS Therapy System.)
Lot codes and dates
    • Product #: 5162-00 Serial #'s: 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
Amount recalled
27 (including 2 demos)

Where it was sold

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:51 PM UTC

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