CooperSurgical recalls Quantum 2000 Electrosurgical Generators with part numbers 909075, 909075-05, and 909075-05W that may stop cutting, coagulating, or blending during surgery if the 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 Quantum 2000 Electrosurgical Generators with specific part numbers and serial ranges that may stop working during surgery when the foot pedal is activated. This could lead to incomplete procedures or complications if the device fails mid-operation.
The generator may stop cutting, coagulating, or blending during surgery when the foot pedal is pressed. This could cause incomplete procedures or complications if the device fails mid-operation. The issue occurs due to a potential malfunction in the device's electrical system.
Surgical teams using the Quantum 2000 Electrosurgical Generator with part numbers 909075, 909075-05, or 909075-05W are most at risk during procedures. The hazard affects devices sold between 2015 and 2017.
Check for part numbers 909075, 909075-05, or 909075-05W on the generator. Serial numbers range from 2015120001 to 2017080010 across multiple production batches from 2015 to 2017.
Look for part numbers 909075, 909075-05, or 909075-05W on the generator.
Reach out to CooperSurgical for guidance on next steps if you have the recalled device.
Part numbers 909075, 909075-05, and 909075-05W are affected.
Serial numbers range from 2015120001 to 2017080010 across multiple production batches from 2015 to 2017.
No immediate stop is required, but you should check the part number and serial number to determine 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-0600-2020 — CooperSurgical CooperSurgical Hello, I own a CooperSurgical that is covered by recall Z-0600-2020 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.
