Reported Jul 5, 2023 · Ongoing
MEGADYNE MEGA SOFT Universal Dual 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 Universal Dual Patient Return Electrode. used during electrosurgery
- Lot codes and dates
- Model No. 0846
- UDI-DI10614559104248; 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.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.