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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: WILSON-COOK MEDICAL INC 6 SHOOTER SAEED MULTI-BAND LIGATOR; LIGATOR, ESOPHAGEAL

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WILSON-COOK MEDICAL INC 6 SHOOTER SAEED MULTI-BAND LIGATOR; LIGATOR, ESOPHAGEAL Back to Search Results
Model Number G31917
Medical Device Problem Code Device Dislodged or Dislocated (2923)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 02/19/2025
Type of Reportable Event Malfunction
Event or Problem Description
During an unspecified ligation procedure, the physician used a cook 6 shooter saeed multi-band ligator.It was reported that one ligature was triggered but did not stay in place [bands falls off varix].An unintended section of the device did not remain inside the patient¿s body.The patient did not require any additional procedures due to this occurrence.According to the initial reporter, the patient did not experience any adverse effects due to this occurrence.
 
Additional Manufacturer Narrative
Investigation evaluation: a product evaluation was not performed in response to this report because the product said to be involved was not provided to cook for evaluation.The report could not be confirmed.The device history record for the lot number said to be involved was reviewed.A discrepancy or anomaly was not observed with the product that was released for distribution.Investigation conclusion: we could not conduct a complete investigation because the product said to be involved was not returned for evaluation.A definitive cause for the reported observation could not be determined.Slippage of the band from the varix can occur if the endoscope is advanced beyond the banded site.The instructions for use caution the user: "passing endoscope over a previously placed band may dislodge band." prior to distribution, all 6 shooter saeed multi-band ligators are subjected to a visual inspection to ensure device integrity.A review of the device history record confirmed that the lot said to be involved met all manufacturing requirements prior to shipment.Corrective action: based on the quality engineering risk assessment no corrective action is warranted at this time.A review of the complaint history was conducted.Based on this review, the likelihood of this type of report is rare.Quality assurance will continue to monitor for complaint trends.
 
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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
3367440157
MDR Report Key21646592
Report Number1037905-2025-00216
Device Sequence Number7614909
Product Code MND
UDI-Device Identifier00827002319172
UDI-Public(01)00827002319172(17)250408(10)W4826168
Combination Product (Y/N)N
Initial Reporter CountryCH
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source Foreign,Health Professional,Company Representative
Initial Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date (Section B) 03/19/2025
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 Expiration Date04/08/2025
Device Model NumberG31917
Device Catalogue NumberMBL-U-6
Device Lot NumberW4826168
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 02/20/2025
Initial Report FDA Received Date03/19/2025
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured04/08/2024
Usage of Device Initial
Patient Sequence Number1
Concomitant Medical Products
and Therapy/Usage Dates
SCOPE, UNKNOWN MAKE AND MODEL.
Patient SexUnknown
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