Cooper Surgical recalls LEEP PRECISION Generator 220V (part LP-20-220) due to potential coagulation failure during use, requiring medical intervention for bleeding. Affected units have specific serial numbers.
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.
Cooper Surgical is recalling their LEEP PRECISION Generator 220V devices because the coagulation function might not work properly with the Hand Switch. This could cause bleeding during surgery that needs medical help to stop.
The device's coagulation function may not operate correctly when the Hand Switch is used. This can lead to uncontrolled bleeding during surgery that requires medical intervention to stop.
Surgical professionals using the LEEP PRECISION Generator 220V for medical procedures are most at risk if the coagulation function fails during surgery.
Check for the part number LP-20-220 and serial numbers starting with 2018100001, 2018100002, or 2018100003 on the device.
Look for serial numbers starting with 2018100001, 2018100002, or 2018100003 on the device.
The device may not coagulate tissue properly with the Hand Switch, which could lead to bleeding requiring medical intervention during surgery.
The official recall does not specify a remedy; check the serial number to see if it's affected.
Look for the part number LP-20-220 and serial numbers starting with 2018100001, 2018100002, or 2018100003.
We’ve drafted a message you can send Cooper Surgical to request your refund or repair — edit it as you like.
Subject: Recall Z-0260-2022 — Cooper Surgical Cooper Surgical Hello, I own a Cooper Surgical that is covered by recall Z-0260-2022 from Cooper Surgical. 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.
