# FDA recall Z-1352-2018

> **The Magstim Company Limited** · Class II · device recall initiated 2017-09-28.

## 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

## Distribution

US Nationwide Distribution in the states of AR, CA, GA, KS, MA, MD, MO, NC, NJ, NW, NY, TX and Hawaii

## Key facts

- **Recall number:** Z-1352-2018
- **Recalling firm:** The Magstim Company Limited
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-09-28
- **Report date:** 2018-04-18
- **Termination date:** 2022-06-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Whitland, United Kingdom

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1352-2018

## Citation

> AI Analytics. FDA recall Z-1352-2018. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1352-2018. Source: US FDA. Licensed CC0.

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