LEEP PRECISION GeneratorRecalls & reported problems across all models
Coopersurgical, Inc. · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 46
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls
- 0
We found 2 models of LEEP PRECISION Generator by Coopersurgical, Inc. in the FDA's device registry (GUDID). Together they are named in 46 adverse event reports in the FDA's MAUDE database, received between May 7, 2022 and Jul 30, 2026 — classified as 1 injury, 45 malfunctions.
The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (41 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported LEEP PRECISION Generator problems
Device problems
- Electrical /Electronic Property Problem41
- Mechanical Problem10
- Insufficient Device Problem Information1
- Output Problem1
- Therapeutic or Diagnostic Output Failure1
- Unintended Electrical Shock1
Patient problems
- No Clinical Signs, Symptoms or Conditions44
- Hemorrhage/Blood Loss/Bleeding2
LEEP PRECISION Generator models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- LEEP PRECISION™ Generator LP-20-120Electrocautery, Gynecologic (And Accessories)45 reports
- LEEP PRECISION™ Generator DMLP-20-120Electrocautery, Gynecologic (And Accessories)1 report
Recent LEEP PRECISION Generator adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionJul 30, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50083838 ↗MalfunctionApr 21, 2026Electrical /Electronic Property Problem
IT WAS REPORTED THAT THE LEEP UNIT WOULD NOT CUT OR BLEND. THERE WAS A BURNED SMELL WHEN CASE COVER REMOVED. UNIT TO BE RETURNED FOR REPAIR. NO ADDITIONAL INFORMATION AVAILABLE. 1216677-2026-00033 LP-20-120 LEEP (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24944913 ↗MalfunctionJan 23, 2026Electrical /Electronic Property Problem
NO ADDITIONAL INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24160380 ↗MalfunctionJan 6, 2026Electrical /Electronic Property Problem
IT WAS REPORTED THAT THERE IS NO POWER GOING TO WAND. THE UNIT GETS NO OUTPUT. NO PATIENT HARM REPORTED. DEVICE BEING RETURNED FOR REPAIR. NO ADDITIONAL INFORMATION. LP-20-120 LEEP 2025-12-0000327.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23974845 ↗MalfunctionDec 16, 2025Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
NO ADDITIONAL INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23817790 ↗MalfunctionNov 24, 2025Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
NO ADDITIONAL INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23635857 ↗MalfunctionNov 5, 2025Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
NO ADDITIONAL INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23475510 ↗MalfunctionNov 5, 2025Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
NO ADDITIONAL INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23475407 ↗MalfunctionJul 1, 2025Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
NO ADDITIONAL INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22373510 ↗MalfunctionMay 13, 2025Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
IT WAS REPORTED THAT DURING AN UNKNOWN PROCEDURE ON (B)(6) 2025, THE LEEP DEVICE GAVE AN R/F ERROR WHEN ATTEMPTING TO COAG. THEY WERE ABLE TO BLEND AND CUT FINE BUT GOT AN ERROR WHEN ATTEMPTING TO COAG. NO PATIENT HARM. NO ADDITIONAL INFORMATION AVAILABLE. DEVICE TO BE RETURNED FOR REPAIR. LP-20-120 (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22009152 ↗MalfunctionMay 12, 2025Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
NO ADDITIONAL INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22002160 ↗MalfunctionMay 12, 2025Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
IT WAS REPORTED THAT DURING AN UNKNOWN PROCEDURE, THE LEEP UNIT SHUT OFF MID-PROCEDURE. THE DOCTOR FINISHED THE PROCEDURE WITH MANUAL REMOVAL OF TISSUE. NO PATIENT INJURY REPORTED. NO ADDITIONAL INFORMATION IS AVAILABLE. DEVICE TO BE RETURNED FOR REPAIR. LP-20-120 LEEP (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22002159 ↗MalfunctionApr 30, 2025Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
NO ADDITIONAL INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21937679 ↗MalfunctionApr 30, 2025Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
NO ADDITIONAL INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21935238 ↗MalfunctionApr 29, 2025Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
NO ADDITIONAL INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21930184 ↗
Other Coopersurgical, Inc. products
All Coopersurgical, Inc. devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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