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The Magstim Company Limited recalls Magstim Rapid Therapy System consisting of: Rapid Mainframe, Rapid Single Power Supply Unit , Rapid User Interface, Air
Recalled April 18, 2018 · FDA recall Z-1352-2018 · The Magstim Company
Hazard
Users manuals not supplied with 4800-00T US Rapid Therapy System · FDA Class II
Units
43
Sold at
US Nationwide Distribution in the states of AR, CA, GA, KS, MA, MD, MO, NC, NJ, NW, NY, TX and Hawaii
Description
Users manuals not supplied with 4800-00T US Rapid Therapy System
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.
Manufacturer(s)
The Magstim Company Limited
Made in
United Kingdom
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →