LEEP Precision Integrated System 120V & LEEP Precision Generator — Class II medical device recall Z-2057-2019
Terminated recall by CooperSurgical, Inc., reported 2019-07-31, distributed nationwide. The products' cut, coagulate, or blend function may not operate with the use of the Foot Pedal.
| Recall number | Z-2057-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CooperSurgical, Inc., Trumbull, CT, United States |
| Recall initiated | 2019-06-18 |
| Classified | 2019-07-23 |
| Reported by FDA | 2019-07-31 |
| Terminated | 2020-06-15 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CR |
| Quantity | 358 |
| Serial numbers | 1214007, 2015080015, 2015110007, 2015110019, 2016030001, 2016030002, 2016030003, 2016030004, 2016030005, 2016030006, 2016030007, 2016030008, 2016030009, 2016030010, 2016030011, 2016030012, 2016030013, 2016030014, 2016030015, 2016030016, 2016030017, 2016040001, 2016040002, 2016040003, 2016040004 and 333 more |
| Model numbers | LP-10-120, LP-20-120 |
Product
LEEP Precision Integrated System 120V & LEEP Precision Generator, Model Nos. LP-10-120 & LP-20-120
Reason for recall
The products' cut, coagulate, or blend function may not operate with the use of the Foot Pedal.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2057-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.