Reported Nov 24, 2021 · Ongoing
LEEP PRECISION Generator 120V Cooper Surgical Part Number: 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 Generator 120V
- Cooper Surgical Part NumberLP-20-120
- Lot codes and dates
- Serial Numbers
227 of 227 codes
021500212140072015050001201606003020160600312016070002201607000420160700122016070017201607002120160700222016070026201607002720160700282016070030201607003120160800022016080004201608000720160800092016080015201608001620160800172016080018201608001920160800202016080021201608002220160800252016080026201608002720160800292016080031201608003320160800342016080035201608003620161000022016100004201610000920161000102016100012201610001320161000142016100016201610001720161000182016100021201610002320161000242016100025201610002720161000282015050016201505001720150500182015050019201505002020151100072016030001
- Serial Numbers
- Amount recalled
- 244 Units
This recall covers 7 products
The agency filed one notice per product. You are reading one of them; the other 6 are below.
Where it was sold
- Nationwide
- PR
Why it was 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.
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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