Home / Recalls / Medical Devices
CooperSurgical, Inc. recalls LEEP Precision Integrated System 120V & LEEP Precision Generator, Model Nos. LP-10-120 & LP-20-120
Recalled July 31, 2019 · FDA recall Z-2057-2019 · CooperSurgical
Hazard
The products' cut, coagulate, or blend function may not operate with the use of the Foot Pedal. · FDA Class II
Units
358
Sold at
Nationwide domestic distribution. International distribution to Canada and Costa Rica.
Description
The products' cut, coagulate, or blend function may not operate with the use of the Foot Pedal.
Product
LEEP Precision Integrated System 120V & LEEP Precision Generator, Model Nos. LP-10-120 & LP-20-120
Manufacturer(s)
CooperSurgical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →