Reported Nov 24, 2021 · Ongoing

Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075

CooperSurgical, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: CooperSurgical, Inc. · 95 Corporate Dr · Trumbull, CT · 06611-1350

Is this the product you have?

  • Quantum 2000 Electrosurgical
  • Generators Cooper Surgical Part Number909075
Lot codes and dates
  • Serial Numbers
    • 0112010
    • 0209001
    • 0214002
    • 0309031
    • 0313007BFIX
    • 0411002
    • 0609010FIX
    • 0710001
    • 0711008
    • 0713011C
    • 0809009
    • 0813032CFIX
    • 091402
    • 1013009C
    • 1013015C
    • 1109017
    • 1214005
    • 2015090019
    • 2015110003
    • 2016030001
    • 2016040012
    • 2016060016
    • 2016090003
    • 2016110002
    • 2017010005
    • 2017060010
    • 2017080010
    • QTMAA-4-095
    • QTM-AB-10-149
    • QTM-M-4-102FIX
    • W110954
    • W351106
    • W60413
    • 0114011
    • 0212004
    • 0214007
    • 0312021
    • 0313010B
    • 0413003B
    • 0612001B
    • 0710003
    • 0711008FIX
    • 0713018C
    • 0811017
    • 0813033C
    • 1011010
    • 1013010C
    • 1014004
    • 1111002
    • 2015040009
    • 2015090021
    • 2015110004
    • 2016030002
    • 2016040015
    • 2016060020
    • 2016090004
    • 2016110003
    • 2017020004
    • 2017060013
    AFZFIX

    65 of 65 codes

    • QTMAA4101
    • QTM-AB-12-164
    • QTMY-11-0201
    • W204996
    • W381180
    • W605041
    • 0114013
    • 0212008
    • 0214008
    • 0312024
    • 0313011B
    • 0511002
    • 0612003B
    • 0710008
    • 0711009
    • 0714007
    • 0811021
    • 0813034C
    • 1011010FIX
    • 1013011C
    • 1109008
    • 1213005C
    • 2015060003
    • 2015100004
    • 2015110009
    • 2016040001
    • 2016040018
    • 2016070003
    • 2016090007
    • 2016110004
    • 2017030002
    • 2017080002
    • ATM-AA-4-106
    • QTMAA-4-102
    • QTM-AB-12-165
    • QTMY-12-0208
    • W2A1022
    • W381192
    • W708311FIX
    • 0115006
    • 0212010
    • 0215005
    • 0312033
    • 0409005
    • 0511003
    • 0612010B
    • 0710008FIX
    • 0712009B
    • 0809004
    • 0811021FIX
    • 0814011FIX
    • 1012006B
    • 1013012C
    • 1109014
    • 1213006C
    • 2015090012
    • 2015100006FIX
    • 2015110010
    • 2016040002
    • 2016060012
    GHILL
    • QTMAA6116
    • QTMAB3067
    • QTMY70139
    • W2B1036
    • W604009
    • 0115007
    • 0214001
    • 0215007
    • 0313001B
    • 0409006
    • 0511003FIX
    • 0612016B
    • 0711006
    • 0713001C
    • 0809007
    • 0813029C
    • 0814012
    • 1013006C
    • 1013014C
    • 1109015
    • 1214003
    • 2015090015
    • 2015110001
    • 2016020006
    • 2016040007
    • 2016060013
    • 2016080002
    • 2016110001
    • 2017010002
    • 2017030009
    • 2017080006
    • IUY80207
    • QTMAA-6-116
    • QTM-AB-9135
    • W107893
    • W2C1054
    • W604013
Amount recalled
193 Units

This recall covers 7 products

The agency filed one notice per product. You are reading one of them; the other 6 are below.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Coagulate function may not operate with the use of the Hand Switch, failure of the device to coagulate tissue may lead to a prolonged procedure requiring medical intervention to control any intraoperative bleeding and complete the case.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:34 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.