PlainRecalls

The Magstim Company Limited

Compiled from official public sources by the publisher.

6 recalls on record · Latest: Jan 27, 2021

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Agency notice ledger

Federal filing book The Magstim Company Limited LIGHT-BOOK · SINGLE-AGENCY

#2,316 of 14,151 · 6 notices · 0.006% archive

  • BOOK 6 notices
  • RANK #2,316 of 14,151
  • SHARE 0.006% archive
  • AGENCY FDA Devices (6)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jan 27, 2021
  • PHOTO 1908 Brands

Nearest notice-volume peer: 1908 Brands (0 notice gap)

The Magstim Company Limited accounts for about 0.006% of the 104,423-notice archive on 6 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

How The Magstim Company Limited compares to 14,151 recalling firms

The Magstim Company Limited ranks 2,316th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

The Magstim Company Limited vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

6 2316th of 14151 higher than 11,804 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-15

The Magstim Company Limited in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows The Magstim Company Limited holds about 0.006% of archive notices alongside 6 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jan 27, 2021

Neurosign 100, Product Number 9883-01. Intraoperative Nerve Monitor - Product Usage: indicated for use in stimulating and monitoring cranial motor nerves, especially the facial nerve (VII), during ENT surgical procedures.
FDA Devices Moderate Sep 2, 2020

Neurosign V4 Intraoperative Nerve monitor family of devices.
FDA Devices Moderate May 20, 2020

Horizon PSU Stim Interconnecting Cable - Product Usage: Horizon is indicated for the treatment of Major Depressive Disorder in adult patients who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode.
FDA Devices Moderate May 20, 2020

Rapid2 PSU Stim Interconnecting Cable - Product Usage: indicated for the treatment of Major Depressive Disorder in adult patients who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode.
FDA Devices Moderate Feb 20, 2019

HORIZON Ez Arm (Part of the HORIZON TMS Therapy System.)
FDA Devices Moderate Apr 18, 2018

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.

The Magstim Company Limited holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar recall count

Nearest multi-notice firms by distinct-event totals (6 here).

1908 Brands 6 Abbott Molecular 6 Accriva Diagnostics, Inc. 6 Advance Medical Designs, Inc. 6 Agave Dream 6

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Abbott Molecular 6 Accriva Diagnostics, Inc. 6 Advance Medical Designs, Inc. 6 American Medical Systems, Inc. 6

Frequently Asked Questions

How many federal recall notices name The Magstim Company Limited? ▼
PlainRecalls indexes 6 distinct federal recall events naming The Magstim Company Limited, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does The Magstim Company Limited sit among other recalling firms? ▼
The Magstim Company Limited ranks #2,316 of 14,151 by distinct recall-event count among 14,151 firms in this archive (83rd percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of The Magstim Company Limited's notices? ▼
FDA Devices accounts for 6 of this firm's 6 indexed notices.
What product category dominates The Magstim Company Limited's filing book? ▼
Filings for The Magstim Company Limited span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
The Magstim Company Limited: 6 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming The Magstim Company Limited; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026