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Megadyne Medical Products, Inc. recalls MegaPower Electrosurgical Generator, Product code 1000, GTIN 10614559103715
Recalled August 22, 2018 · FDA recall Z-2792-2018 · Megadyne Medical Products
Hazard
If two devices are plugged into the same channel/port in the generator, both devices activate. If one device is left laying on the patient, the result could be burning of the patient. · FDA Class II
Units
8380 units
Sold at
Worldwide distribution. US Nationwide, Mexico, Europe, Middle East, Latin America, Africa, and Asia Pacific Markets
Description
If two devices are plugged into the same channel/port in the generator, both devices activate. If one device is left laying on the patient, the result could be burning of the patient.
Product
MegaPower Electrosurgical Generator, Product code 1000, GTIN 10614559103715
Manufacturer(s)
Megadyne Medical Products, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →