Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LEEP PRECISION Integrated System Recalled by CooperSurgical, Inc. Due to Coagulate function may not operate with the use...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact CooperSurgical, Inc. directly.
Affected Products
LEEP PRECISION Integrated System, 120V CooperSurgical part number: LP-10-120
Quantity: 1587 Units
Why Was This 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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About CooperSurgical, Inc.
CooperSurgical, Inc. has 83 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report