Users manuals not supplied with 4800-00T US Rapid Therapy System
Users manuals not supplied with 4800-00T US Rapid Therapy System
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send The Magstim Company Limited to request your refund or repair — edit it as you like.
Subject: Recall Z-1352-2018 — The Magstim Company Limited The Magstim Company Limited recalls Magstim Rapid Therapy System consis Hello, I own a The Magstim Company Limited recalls Magstim Rapid Therapy System consisting of: Rapid Mainframe, Rapid Single Power Supply Unit , Rapid User Interface, Air that is covered by recall Z-1352-2018 from The Magstim Company Limited. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
