Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Magstim Rapid Therapy System consisting of: Rapid Mainframe Recalled by The Magstim Company Limited Due to Users manuals not supplied with 4800-00T US Rapid...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact The Magstim Company Limited directly.
Affected Products
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.
Quantity: 43
Why Was This Recalled?
Users manuals not supplied with 4800-00T US Rapid Therapy System
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About The Magstim Company Limited
The Magstim Company Limited has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report