Reported Jul 10, 2024 · Ongoing

Brand Name: MEGADYNE" MEGA 2000" Patient Return Electrode Product Name: MEGADYNE" MEGA 2000" Patient Return Electrode…

Megadyne Medical Products, Inc.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Megadyne Medical Products, Inc. · 4545 Creek Rd · Blue Ash, OH · 45242-2803

Is this the product you have?

  • Brand NameMEGADYNE" MEGA 2000"
  • Patient Return Electrode Product NameMEGADYNE" MEGA 2000" Patient
  • Return Electrode Model/Catalog Number0800
  • Software VersionN/A
  • Product Description
    • Reusable Patient Return Electrode
    • Mega 2000
    • Adult
    • For Patients Weighing over 25lbs. (11.4Kg)
    • 91cm
  • Long x 51cm Wide ComponentNo
Lot codes and dates
  • Product Code0800
  • UDI-DI10614559100936
  • Lot NumberAll distributed lot numbers. Product code has been discontinued from future production
Amount recalled
259 units

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

  • Nationwide

Why it was recalled

Stop using this product now

To limit the use of the Mega Soft Pads to patients aged 12 or older to mitigate the potential risk of patient burns identified with use of Mega Soft pads.

Using this product could cause serious injury, illness or death — stop using it now.

Want the full recall guide?

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:34 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.