Class II — The Magstim Company Limited
| Recalling firm | The Magstim Company Ltd. |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | A stray strand of stainless-steel cable may protrude from the heat shrink sleeving on the Balance Cable of the Ez Arm. |
| Product | HORIZON Ez Arm (Part of the HORIZON TMS Therapy System.) |
| Quantity | 27 (including 2 demos) |
| Distribution | CA, MA, MN, PA, TX, VA, WI, and WA |
| Initiated | 2018-10-25 |
| Classified | 2019-02-14 |
| Recall number | Z-0836-2019 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — The Magstim Company Limited (Z-0836-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/81489/
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