# FDA recall Z-1966-2020

> **The Magstim Company Limited** · Class II · device recall initiated 2020-03-23.

## Product

Rapid2 PSU   Stim Interconnecting Cable - Product Usage: 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.

## Distribution

Worldwide distribution - US Nationwide distribution including in the states of AL, AR, CA, CT, TN, IL, MN, MT, NC, NJ, NY, PA, SC, TX, WA, and the countries of Cyprus, China, Iran, Saudi Arabia, UK, Italy, Malaysia, Spain, Taiwan, Vietnam, Australia, Japan, Turkey, France and Israel.

## Key facts

- **Recall number:** Z-1966-2020
- **Recalling firm:** The Magstim Company Limited
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-03-23
- **Report date:** 2020-05-20
- **Termination date:** 2024-09-20

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1966-2020

## Citation

> AI Analytics. FDA recall Z-1966-2020. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-1966-2020. Source: US FDA. Licensed CC0.

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