LEEP PRECISION™ Generator DMLP-20-120Recalls & reported problems
Coopersurgical, Inc. · LEEP PRECISION™ Generator (120 VAC) · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888937019926), received between Jun 2, 2023 and Jun 2, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (1 report).
9 other recalls cover devices cleared under the same FDA submission (K963653); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Electrical /Electronic Property Problem1
- Mechanical Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 2, 2023Electrical /Electronic Property Problem; Mechanical Problem; Electrical /Electronic Property Problem; Mechanical Problem
NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17050265 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K963653. One submission often covers many models, so check the product and lot details in each record.
- Z-0263-2022 · Sep 29, 2021 · Open, ClassifiedQuantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075-05W
- Z-0261-2022 · Sep 29, 2021 · Open, ClassifiedQuantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075
- Z-0260-2022 · Sep 29, 2021 · Open, ClassifiedLEEP PRECISION Generator 220V Cooper Surgical Part Number: LP-20-220
- Z-0259-2022 · Sep 29, 2021 · Open, ClassifiedLEEP PRECISION Generator 120V Cooper Surgical Part Number: LP-20-120
- Z-0262-2022 · Sep 29, 2021 · Open, ClassifiedQuantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075-05
- Z-0600-2020 · Oct 16, 2019 · TerminatedQuantam 2000 Electrosurgical Generator, Part number 909075.
- Z-0602-2020 · Oct 16, 2019 · TerminatedQuantam 2000 Electrosurgical Generator, Part number 909075-05W.
- Z-0601-2020 · Oct 16, 2019 · TerminatedQuantam 2000 Electrosurgical Generator, Part number 909075-05.
- Z-2057-2019 · Jun 18, 2019 · TerminatedLEEP Precision Integrated System 120V & LEEP Precision Generator, Model Nos. LP-10-120 & LP-20-120
Other Electrocautery, Gynecologic (And Accessories) devices
- Enseal NSLX137CEthicon Endo-Surgery, LLC · ELECTROCAUTERY, GYNECOLOGIC (AND ACCESSORIES)3 deaths344 reports
- ENSEAL X1 NSLX120LEthicon Endo-Surgery, LLC · ELECTROCAUTERY, GYNECOLOGIC (AND ACCESSORIES)2 deaths172 reports
- Fischer Cone Biopsy Excisor 900-157Coopersurgical, Inc. · Electrocautery, Gynecologic (And Accessories)1 recall0 reports
- LEEP PRECISION™ Generator LP-20-120Coopersurgical, Inc. · Electrocautery, Gynecologic (And Accessories)45 reports
- Harmonic NSLX137SEthicon Endo-Surgery, LLC · ELECTROCAUTERY, GYNECOLOGIC (AND ACCESSORIES)1 death19 reports
- LEEP PRECISION™ Integrated System LP-10-120Coopersurgical, Inc. · Electrocautery, Gynecologic (And Accessories)12 reports
- Fischer Cone Biopsy Excisor 900-151Coopersurgical, Inc. · Electrocautery, Gynecologic (And Accessories)10 reports
- AESCULAP PM438RAesculap AG · ELECTROCAUTERY, GYNECOLOGIC (AND ACCESSORIES)7 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.