PlainRecalls

Megadyne Medical Products, Inc.

20 recalls on record · Latest: Jul 10, 2024

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Agency notice ledger

Federal filing book Megadyne Medical Products,… MID-BOOK · SINGLE-AGENCY

#811 of 14,151 · 20 notices · 0.019% archive

  • BOOK 20 notices
  • RANK #811 of 14,151
  • SHARE 0.019% archive
  • AGENCY FDA Devices (20)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jul 10, 2024
  • PHOTO AbbVie Inc.

Nearest notice-volume peer: AbbVie Inc. (0 notice gap)

Megadyne Medical Products, Inc. accounts for about 0.019% of the 104,423-notice archive on 20 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 Megadyne Medical Products,… compares to 14,151 recalling firms

Megadyne Medical Products, Inc. ranks 811th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Megadyne Medical Products,… vs all firms by recall-notice count

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

20 811th of 14151 higher than 13,326 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 · 2026-09-13

Megadyne Medical Products,… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Megadyne Medical Products, Inc. holds about 0.019% of archive notices alongside 20 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Critical Jul 10, 2024

Brand Name: MEGADYNE" MEGA SOFT" Reusable Patient Return Electrode Product Name: MEGADYNE" MEGA SOFT" Reusable Patient Return Electrode Model/Catalog Number: 0830 Software Version: N/A Product Description: Reusable Patient Return Electrode, Mega Soft, Single Cord, Adult, For Patients Weighing over 25lbs (11.4Kg), 117cm Long x 51cm Wide x 1.25cm Thick Component: No

FDA Devices Critical Jul 10, 2024

Brand Name: MEGADYNE" MEGA 2000" Patient Return Electrode Product Name: MEGADYNE" MEGA 2000" Patient Return Electrode Model/Catalog Number: 0800 Software Version: N/A Product Description: Reusable Patient Return Electrode, Mega 2000, Adult, For Patients Weighing over 25lbs. (11.4Kg), 91cm Long x 51cm Wide Component: No

FDA Devices Critical Jul 10, 2024

Brand Name: MEGADYNE" MEGA SOFT" Dual Reusable Patient Return Electrode Product Name: MEGADYNE" MEGA SOFT" Dual Reusable Patient Return Electrode Model/Catalog Number: 0835 Software Version: N/A Product Description: Reusable Patient Return Electrode, Mega Soft, Dual Cord, Adult, For Patients Weighing over 25lbs. (11.4kg), 117cm Long x 51cm Wide x 1.25cm Thick Component: No

FDA Devices Critical Jun 12, 2024

MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. Reusable Patient Return Electrode for patients weighing (0.8lb-50lb), (350g-22.7Kg), 66cm Long x 30.5cm Wide x 1.25cm. Electrosurgical use.

FDA Devices Critical Jan 3, 2024

Product Code 0848, MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode, Reusable Patient Return Electrode, Mega Soft Universal Dual Plus

FDA Devices Critical Jan 3, 2024

Product Code 0847, MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode, Reusable Patient Return Electrode, Mega Soft Universal Plus

FDA Devices Critical Jan 3, 2024

Product Code 0846, MEGADYNE MEGA SOFT Universal Dual Patient Return Electrode, Reusable Patient Return Electrode, Mega Soft Universal Dual Cord

FDA Devices Critical Jan 3, 2024

Product Code 0845, MEGADYNE MEGA SOFT Universal Patient Return Electrode, Reusable Patient Return Electrode

FDA Devices Moderate Aug 9, 2023

MEGADYNE Suction Coagulators, Product Code 004125 (Suction Coagulator, Handswitching, 10 Fr, 6 inch (15.24cm)), Product Code 004225 (Suction Coagulator, Handswitching, 8 Fr, 6 inch (15.24cm), Product Code 004325 (Suction Coagulator, Handswitching, 12 Fr, 6 inch (15.24cm)), and Product Code 0041BN (Suction Coagulator, Handswitching, 10 Fr, 6 inch (15.24cm), Bulk Non Sterile)

FDA Devices Critical Jul 5, 2023

MEGADYNE MEGA SOFT Universal Dual Patient Return Electrode. used during electrosurgery

FDA Devices Critical Jul 5, 2023

MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode. used during electrosurgery

FDA Devices Critical Jul 5, 2023

MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. used during electrosurgery

FDA Devices Critical Jul 5, 2023

MEGADYNE MEGA 2000 Patient Return Electrode. used during electrosurgery

FDA Devices Critical Jul 5, 2023

MEGADYNE MEGA SOFT Reusable Patient Return Electrode. used during electrosurgery

FDA Devices Critical Jul 5, 2023

MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode. used during electrosurgery

FDA Devices Critical Jul 5, 2023

MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrode. used during electrosurgery

FDA Devices Critical Jul 5, 2023

MEGADYNE MEGA SOFT Universal Patient Return Electrode. used during electrosurgery

FDA Devices Moderate Aug 22, 2018

MegaPower Electrosurgical Generator, Product code 1000, GTIN 10614559103715

FDA Devices Moderate Mar 19, 2014

Hand Control 12FR Suction Coagulator with 10 ft cord and holster, Sterile, Disposable, Model Number 0043-25, packaged Tyvek¿ polyester peel pouch, 25 pouches per box. This device is intended to conduct monopolar electrosurgical energy from an electrosurgical generator (ESU) to target tissue during ENT and general surgical procedures. It is also a suction apparatus used to remove surgical smoke and fluids from the site. The device is intended for single use; it is not intended to be cleaned or

FDA Devices Moderate Sep 4, 2013

E-Z Clean¿ Disposable Laparoscopic Electrode Model Number 0100L and 0100LS. Expiration dates of 05/2018 to 07/2018. Sterile. RX ONLY. This product is packaged individually in a chevron Tyvek¿ - polyester peel pouch, 6 pouches per box. The E-Z Clean laparoscopic electrode is intended to conduct monopolar electrosurgical energy from an electrosurgical generator to target tissue during laparoscopic surgical procedures. This device is intended to be used whenever monopolar electrosurgical cutti

Megadyne Medical Products,… 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 (20 here).

Similar medical devices volume

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

Frequently Asked Questions

How many federal recall notices name Megadyne Medical Products,…?
PlainRecalls indexes 20 distinct federal recall events naming Megadyne Medical Products, Inc., 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 Megadyne Medical Products,… sit among other recalling firms?
Megadyne Medical Products, Inc. ranks #811 of 14,151 by distinct recall-event count among 14,151 firms in this archive (94th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Megadyne Medical Products,…'s notices?
FDA Devices accounts for 20 of this firm's 20 indexed notices.
What product category dominates Megadyne Medical Products,…'s filing book?
Filings for Megadyne Medical Products, Inc. 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.
Megadyne Medical Products, Inc.: 20 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 Megadyne Medical Products, Inc.; individual notices remain authoritative on each linked recall page.

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