FDA Recall Terminated

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.

Recall: Z-1352-2018 · Initiated September 28, 2017

Recall

Recall Number
Z-1352-2018
Event Number
79577
Firm
The Magstim Company Limited Spring Gardens Whitland United Kingdom
FEI Number
3002808356
Product Code
OBP
Status
Terminated
Root Cause
Employee error
Initiated
September 28, 2017
Terminated
June 21, 2022

Description

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

Users manuals not supplied with 4800-00T US Rapid Therapy System

Action

On September 28, 2017 the recalling firm sent a Field Safety Notice that included the Operating Manual to all their customers involved in this event. An Acknowledgement card was attached to the letter to be sent back to the recalling firm informing that they received the Operating Manual

Distribution

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

Quantity

43