CooperSurgical recalls LEEP Precision Integrated System (220V) with part numbers LP-10-220. Failure to coagulate tissue during use may cause prolonged bleeding requiring medical intervention.
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.
CooperSurgical is recalling a specific LEEP Precision Integrated System (220V) model that may not properly coagulate tissue during medical procedures. This could lead to extended surgery times and the need for medical intervention to control bleeding.
The device's coagulation function may not work correctly when the Hand Switch is used. This can cause bleeding during surgery that requires additional medical steps to stop, potentially prolonging the procedure.
Medical professionals using the LEEP Precision system for procedures involving tissue removal. Patients undergoing these procedures are at risk if the device fails to coagulate tissue properly.
Check for part numbers LP-10-220 on the device. The serial numbers listed in the recall include specific dates and sequences from 2017 to 2021.
Look for the part number LP-10-220 on the device to confirm if it is affected.
Reach out to CooperSurgical directly for further instructions or to confirm if your device needs repair.
The recalled device is the LEEP Precision Integrated System (220V) with part number LP-10-220.
Check for the part number LP-10-220 on the device. Affected units have serial numbers listed in the recall from 2017040001 to 2021010005.
Contact CooperSurgical directly for instructions on next steps, as the recall does not specify a repair or replacement process.
We’ve drafted a message you can send CooperSurgical to request your refund or repair — edit it as you like.
Subject: Recall Z-0258-2022 — CooperSurgical CooperSurgical Hello, I own a CooperSurgical that is covered by recall Z-0258-2022 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.
