HORIZON Ez Arm — Class II medical device recall Z-0836-2019
Ongoing recall by The Magstim Company Limited, reported 2019-02-20, distributed in CA, MA, MN, PA, TX, VA, WA, WI. A stray strand of stainless-steel cable may protrude from the heat shrink sleeving on the Balance Cable of the
| Recall number | Z-0836-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | The Magstim Company Limited, Whitland, N/A, United Kingdom |
| Recall initiated | 2018-10-25 |
| Classified | 2019-02-14 |
| Reported by FDA | 2019-02-20 |
| Distributed | CA, MA, MN, PA, TX, VA, WA, WI |
| Serial numbers | 55308/001, 55308/002, 55310/001, 55310/002, 55446/001, 55446/002, 55447-002, 55447/001, 55631-001, 55631-002, 55631-003, 55631-004, 55632/001, 55632/002, 55632/003, 55632/004, 55841-002, 55841-003, 55841-004, 55841/001, 55842/001, 55842/002, 55842/003, 55842/004, 55843-001 and 2 more |
Product
HORIZON Ez Arm (Part of the HORIZON TMS Therapy System.)
Reason for recall
A stray strand of stainless-steel cable may protrude from the heat shrink sleeving on the Balance Cable of the Ez Arm.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0836-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.