Magstim Rapid Therapy System consisting of: Rapid Mainframe — Class II medical device recall Z-1352-2018
Terminated recall by The Magstim Company Limited, reported 2018-04-18, distributed nationwide. Users manuals not supplied with 4800-00T US Rapid Therapy System
| Recall number | Z-1352-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | The Magstim Company Limited, Whitland, United Kingdom |
| Recall initiated | 2017-09-28 |
| Classified | 2018-04-10 |
| Reported by FDA | 2018-04-18 |
| Terminated | 2022-06-21 |
| Distributed | Nationwide (US) |
| Quantity | 43 |
| Model numbers | 4800-00T |
Product
Magstim Rapid Therapy System consisting of: Rapid Mainframe, Rapid Single Power Supply Unit , Rapid User Interface, Air Film Coil and Main Filters Product Usage For the treatment of major depressive disorders in adult patients who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode.
Reason for recall
Users manuals not supplied with 4800-00T US Rapid Therapy System
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-1352-2018. 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.