FDA Device recall Z-2057-2019
LEEP Precision Integrated System 120V & LEEP Precision Generator, Model Nos
- FDA Device
- Class II
- terminated
- Published 2019-07-31
On 2019-07-31 the FDA classified a Class II recall of LEEP Precision Integrated System 120V & LEEP Precision Generator, Model Nos by Coopersurgical, citing the products' cut, coagulate, or blend function may not operate with the use of the Foot Pedal.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2057-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-06-18 |
| Published | 2019-07-31 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Coopersurgical |
| Distribution | US |
Product
LEEP Precision Integrated System 120V & LEEP Precision Generator, Model Nos. LP-10-120 & LP-20-120
Reason
The products' cut, coagulate, or blend function may not operate with the use of the Foot Pedal.
Identifiers
| code_info | Lot/Serial Numbers: 1214007 2016050014 2016060026 2016080009 2016100021 2017010021 2017050015 2017080013 2015080015 20…Lot/Serial Numbers: 1214007 2016050014 2016060026 2016080009 2016100021 2017010021 2017050015 2017080013 2015080015 2016050015 2016060027 2016080010 2016100023 2017010023 2017050016 2017080014 2015110007 2016050016 2016060028 2016080011 2016100024 2017010024 2017050017 2017080015 2015110019 2016050017 2016060029 2016080012 2016100025 2017020001 2017060001 2017090001 2016030001 2016050018 2016060030 2016080013 2016100026 2017020002 2017060002 2017090003 2016030002 2016050019 2016060031 2016080014 2016100027 2017020003 2017060003 2017090004 2016030003 2016050020 2016070001 2016080015 2016100028 2017020005 2017060004 2017090005 2016030004 2016050021 2016070002 2016080016 2016100029 2017020006 2017060005 2017090006 2016030005 2016050022 2016070003 2016080017 2016100030 2017020007 2017060006 2017090007 2016030006 2016050023 2016070004 2016080018 2016100031 2017020008 2017060007 2017090008 2016030007 2016050024 2016070005 2016080019 2016100032 2017020009 2017060008 2017090009 2016 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2057-2019%22
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