Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LEEP Precision Integrated System 120V & LEEP Precision Generator Recalled by CooperSurgical, Inc. Due to The products' cut, coagulate, or blend function may...
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 & LEEP Precision Generator, Model Nos. LP-10-120 & LP-20-120
Quantity: 358
Why Was This Recalled?
The products' cut, coagulate, or blend function may not operate with the use of the Foot Pedal.
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