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

Recall Z-0602-2020 — Quantam 2000 Electrosurgical Generator, Part number 909075-05W.

U.S. FDA — Device Enforcement · United States · 2019-10-16 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0602-2020
Date of alert
2019-10-16
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
CooperSurgical, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
2015120001
Reported risk: Potential for the Quantum 2000 Electrosurgery Generator, part numbers 909075, 909075-05 and 909075-05W, to cease to either cut, coagulate, or blend during a procedure when the foot pedal is used for activation.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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