Horizon PSU Stim Interconnecting Cable — Class II medical device recall Z-1965-2020
Terminated recall by The Magstim Company Limited, reported 2020-05-20, distributed nationwide. It was identified that there is a potential for the Stim Interconnecting high Voltage Cable located at the rea
| Recall number | Z-1965-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | The Magstim Company Limited, Whitland, N/A, United Kingdom |
| Recall initiated | 2020-03-23 |
| Classified | 2020-05-13 |
| Reported by FDA | 2020-05-20 |
| Terminated | 2024-09-20 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CN, CY, ES, FR, GB, IL, IR, IT, JP, MY, SA, TR, TW, VN |
| Quantity | 71 units |
Product
Horizon PSU Stim Interconnecting Cable - Product Usage: Horizon is indicated for the treatment of Major Depressive Disorder in adult patients who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode.
Reason for recall
It was identified that there is a potential for the Stim Interconnecting high Voltage Cable located at the rear of the Rapid2 and Horizon power supply unit to fail.
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-1965-2020. 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.