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

MAUDE Adverse Event Report: Wilson-Cook Medical Inc 6 Shooter Saeed Multi-Band Ligator; Ligator, Esophageal

  • 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
 

Wilson-Cook Medical Inc 6 Shooter Saeed Multi-Band Ligator; Ligator, Esophageal Back to Search Results
Model Number G22692
Medical Device Problem Code Failure to Fire (2610)
Health Effect - Clinical Code Gastrointestinal Hemorrhage (4476)
Date of Event 07/27/2026
Type of Reportable Event Malfunction
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
6 Shooter Saeed Multi-Band Ligator
Common Device Name
Ligator, Esophageal
Manufacturer (Section D)
Wilson-Cook Medical Inc
4900 bethania station rd
winston salem NC 27105
Manufacturer (Section G)
Wilson-Cook Medical Inc
4900 bethania station rd
winston salem NC 27105
Manufacturer Contact
sabrina o¿brien
4900 bethania station rd
winston salem, NC 27105
+1(336)744-0157
MDR Report Key50436708
Report Number1037905-2026-00456
Device Sequence Number10377697
Product Code MND
UDI-Device Identifier00827002226920
Combination Product (Y/N)N
Initial Reporter CountryCH
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Foreign,Company Representative,Distributor
Initial Reporter Occupation Non-Healthcare Professional
Type of Report Initial
Report Date (Section B) 08/25/2026
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 NumberG22692
Device Catalogue NumberMBL-6-F
Device Lot NumberW4992177
Was Device Available for Evaluation? Yes
Date Returned to Manufacturer08/10/2026
Is the Reporter a Health Professional? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 07/28/2025
Initial Report FDA Received Date08/25/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured12/10/2025
Is the Device Labeled for Single Use? (Y/N) Yes
Usage of Device Initial
Patient Sequence Number1
Patient Age55 YR
Patient SexMale
Patient Weight176 LB
-
-