CooperSurgical, Inc.: Medical Device Recall in 2019 - (Recall #: Z-0601-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Quantam 2000 Electrosurgical Generator, Part number 909075-05.

Product Classification:

Class II

Date Initiated: October 16, 2019

Date Posted: December 11, 2019

Recall Number: Z-0601-2020

Event ID: 84132

Reason for Recall:

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.

Status: Terminated

Product Quantity: 110

Code Information:

Serial numbers: 2015120001-2015120030 2016030001-2016030030 2016040001-2016040018 2016050001-2016050030 2016060001-2016060020 2016070001-2016070040 2016080001-2016080006 2016090001-2016090016 2016110001-2016110008 2016120001-2016120006 2017010001-2017010008 2017020001-2017020009 2017030001-2017030011 2017040001-2017040008 2017060001-2017060015 2017080002 2017080006 2017080010

Distribution Pattern:

US: AL, AZ, CA, CO, FL, GA, HI, ID, IL, IN, LA, MA, ME, Ml, MT, ND, NJ, NV, NY, OK, PA, SC, SD, TN, TX, UT, VA, WA, & WV. International: China, Indonesia, South Africa, & Tanzania.

Voluntary or Mandated:

Voluntary: Firm initiated