Reported Jul 31, 2019 · Terminated
LEEP Precision Integrated System 120V & LEEP Precision Generator, Model Nos. LP-10-120 & LP-20-120
CooperSurgical, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: CooperSurgical, Inc. · 95 Corporate Dr · Trumbull, CT · 06611-1350
Is this the product you have?
- LEEP Precision Integrated System 120V & LEEP Precision Generator, Model Nos. LP-10-120 & LP-20-120
- Lot codes and dates
- Lot/Serial Numbers
358 of 358 codes
121400720160500142016060026201608000920161000212017010021201705001520170800132015080015201605001520160600272016080010201610002320170100232017050016201708001420151100072016050016201606002820160800112016100024201701002420170500172017080015201511001920160500172016060029201608001220161000252017020001201706000120170900012016030001201605001820160600302016080013201610002620170200022017060002201709000320160300022016050019201606003120160800142016100027201702000320170600032017090004201603000320160500202016070001201608001520161000282017020005201706000420170900052016030004201605002120160700022016080016
- Lot/Serial Numbers
- Amount recalled
- 358
Where it was sold
- Nationwide
Why it was recalled
The products' cut, coagulate, or blend function may not operate with the use of the Foot Pedal.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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