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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: WILSON-COOK MEDICAL INC (COOK ENDOSCOPY) HERCULES 3 STAGE WIREGUIDED BALLOON ESOPHAGEAL-PYLORIC-COLONIC; DILATOR, ESOPHAGEAL

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WILSON-COOK MEDICAL INC (COOK ENDOSCOPY) HERCULES 3 STAGE WIREGUIDED BALLOON ESOPHAGEAL-PYLORIC-COLONIC; DILATOR, ESOPHAGEAL Back to Search Results
Model Number G51796
Medical Device Problem Code Material Puncture/Hole (1504)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 05/14/2026
Type of Reportable Event Malfunction
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Brand Name
HERCULES 3 STAGE WIREGUIDED BALLOON ESOPHAGEAL-PYLORIC-COLONIC
Common Device Name
DILATOR, ESOPHAGEAL
Manufacturer (Section D)
WILSON-COOK MEDICAL INC (COOK ENDOSCOPY)
4900 bethania station rd
winston salem NC 27105
Manufacturer (Section G)
WILSON-COOK MEDICAL INC (COOK ENDOSCOPY)
4900 bethania station rd
winston salem NC 27105
Manufacturer Contact
sabrina o'brien
4900 bethania station rd
winston salem, NC 27105
3367440157
MDR Report Key25812647
Report Number1037905-2026-00345
Device Sequence Number14940690
Product Code KNQ
UDI-Device Identifier00827002517967
UDI-Public(01)00827002517967(17)290227(10)W5011340
Combination Product (Y/N)N
Initial Reporter CountryCL
Number of Events Summarized1
Summary Report (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) 07/14/2026
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 NumberG51796
Device Catalogue NumberHBD-W-12-13.5-15
Device Lot NumberW5011340
Was Device Available for Evaluation? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 06/17/2026
Initial Report FDA Received Date07/14/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured02/27/2026
Is the Device Labeled for Single Use? (Y/N) Yes
Usage of Device Initial
Patient Sequence Number1
Patient Age72 YR
Patient SexFemale
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