Reported Jul 5, 2023 · Ongoing

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

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?

  • MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrode. used during electrosurgery
Lot codes and dates
  • Model No. 0835
  • UDI-DI10614559101872; All Units
Amount recalled
21,100 units

This recall covers 8 products

The agency filed one notice per product. You are reading one of them; the other 7 are below.

Where it was sold

  • Nationwide

Why it was recalled

Stop using this product now

Firm has received reports of patient burns in surgical procedures where device was used.

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

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Megadyne Medical Products, Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:36 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.