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The Magstim Company Recalls
6 recalls on record · April 18, 2018 to January 27, 2021 · Medical Devices
Recalls by year
18
19
20
21
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
January 27, 2021Medical DevicesFDA
The Magstim Company Limited recalls Neurosign 100, Product Number 9883-01. Intraoperative Nerve Monitor - Product Usage: indicated for use in stimulating an
Hazard: A small number of Neurosign 100 Intraoperative Nerve Monitors may have been dispatched without being configured appropriately for the supply mains within the target Country. The specific deficiency includes: 1. Onboard voltage selector set to 240V (European Standard), versus 120V requirement for the United States and Canada. 2. Fuses installed in the Power Entry Module (PEM) 2xT315mAL (240V Standard), versus the 2xT630mAL requirement for a 120V mains supply.
September 2, 2020Medical DevicesFDA
The Magstim Company Limited recalls Neurosign V4 Intraoperative Nerve monitor family of devices.
Hazard: Reports that manipulation of the cable which connects the pre-amplifier to the nerve monitor, and the cable which connects the pre-amplifier to the stimulator pod, may cause damage to the internal construction of the cables.
May 20, 2020Medical DevicesFDA
The Magstim Company Limited recalls Rapid2 PSU Stim Interconnecting Cable - Product Usage: indicated for the treatment of Major Depressive Disorder in adu
Hazard: 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.
May 20, 2020Medical DevicesFDA
The Magstim Company Limited recalls Horizon PSU Stim Interconnecting Cable - Product Usage: Horizon is indicated for the treatment of Major Depressive Disor
Hazard: 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.
February 20, 2019Medical DevicesFDA
The Magstim Company Limited recalls HORIZON Ez Arm (Part of the HORIZON TMS Therapy System.)
Hazard: A stray strand of stainless-steel cable may protrude from the heat shrink sleeving on the Balance Cable of the Ez Arm.
April 18, 2018Medical DevicesFDA
The Magstim Company Limited recalls Magstim Rapid Therapy System consisting of: Rapid Mainframe, Rapid Single Power Supply Unit , Rapid User Interface, Air
Hazard: Users manuals not supplied with 4800-00T US Rapid Therapy System