CooperSurgical recalls Quantam 2000 Electrosurgical Generators with specific part numbers and serial ranges due to potential failure to cut, coagulate, or blend during procedures when foot pedal is used.
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.
CooperSurgical is recalling Quantam 2000 Electrosurgical Generators with part numbers 909075, 909075-05, and 909075-05W. These devices may stop working during surgery when the foot pedal is activated, which could lead to incomplete procedures.
The generator may stop functioning to cut, coagulate, or blend tissue during surgery when the foot pedal is pressed. This could result in incomplete procedures if the device fails during critical moments.
Surgical staff and hospitals that use the Quantam 2000 Electrosurgical Generator with the specified part numbers and serial ranges are most at risk. This recall affects devices sold between 2015 and 2017.
Check the part number on the generator, which should be 909075, 909075-05, or 909075-05W. Also, verify the serial number falls within the listed ranges from 2015120001 to 2017080010.
Identify the part number on the generator, which should be 909075, 909075-05, or 909075-05W.
Confirm the serial number falls within the specified ranges: 2015120001-2015120030, 2016030001-2016030030, and other ranges listed in the recall.
Part numbers 909075, 909075-05, and 909075-05W are affected.
Serial numbers from 2015120001 to 2017080010, in the specific ranges listed in the recall.
No, but you should check the part number and serial number to confirm if your device is affected.
We’ve drafted a message you can send CooperSurgical to request your refund or repair — edit it as you like.
Subject: Recall Z-0602-2020 — CooperSurgical CooperSurgical Hello, I own a CooperSurgical that is covered by recall Z-0602-2020 from CooperSurgical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
