Product Wiki · Recalls · U.S. FDA — Device Enforcement

MEGADYNE MEGA SOFT Universal Dual Patient Return Electrode. used during electrosurgery — recall Z-2001-2023

U.S. FDA — Device Enforcement · United States · 2023-06-01 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2001-2023
Date of alert
2023-06-01
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Megadyne Medical Products, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10614559104248
Reported risk: Firm has received reports of patient burns in surgical procedures where device was used.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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