Electrode Pad Recall: Megadyne Removes MEGADYNE MEGA SOFT Pediatric Patient Return Electrodes for Risk of Serious Burn Injuries to Patients

Megadyne is recalling MEGADYNE MEGA SOFT Pediatric Patient Return Electrodes after receiving reports of patient burn injuries in procedures where the MEGA SOFT Pediatric Patient Return Electrodes were used.

The U.S. Food and Drug Administration (FDA) has identified this as a Class I recall, the most serious type of recall. Please be aware, this recall involves removing devices from where they are used or sold. Use of these affected devices may causeserious injuries, serious health consequences, or death. 

Questions?

Customers with questions about this recall should contact the Ethicon Resource Department at 1-877-ETHICON (1-877-384-4266).