• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Covidien LigaSure; ELECTROSURGICAL, CUTTING & COAGULATION & ACCES

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

Covidien LigaSure; ELECTROSURGICAL, CUTTING & COAGULATION & ACCES Back to Search Results
Model Number LF1937
Medical Device Problem Codes Device Alarm System (1012); Energy Output Problem (1431); Intermittent Energy Output (4025)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 09/08/2026
Type of Reportable Event Malfunction
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
LigaSure
Common Device Name
ELECTROSURGICAL, CUTTING & COAGULATION & ACCES
Manufacturer (Section D)
Covidien
6044 longbow court
boulder CO 80301 -329
Manufacturer (Section G)
Covidien
6044 longbow court
boulder CO 80301 -329
Manufacturer Contact
mike bocchino
8200 coral sea st ne
mounds view, MN 55112--439
+1(800)646-4633
MDR Report Key50932986
Report Number1717344-2026-01315
Device Sequence Number9597926
Product Code GEI
UDI-Device Identifier10884521705913
Combination Product (Y/N)N
Initial Reporter CountryCA
PMA/510(K) Number
K170869
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Foreign,Health Professional,Company Representative
Initial Reporter Occupation Physician
Type of Report Initial
Report Date (Section B) 09/29/2026
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Operator of Device Health Professional
Device Model NumberLF1937
Device Catalogue NumberLF1937
Device Lot Number61540279X
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 09/08/2026
Initial Report FDA Received Date09/29/2026
Date Device Manufactured06/03/2026
Is the Device Labeled for Single Use? (Y/N) Yes
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Initial
Patient Sequence Number1
Patient SexUnknown
-
-