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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: COOK INC CODA BALLOON CATHETER; DQY CATHETER, PERCUTANEOUS

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COOK INC CODA BALLOON CATHETER; DQY CATHETER, PERCUTANEOUS Back to Search Results
Model Number G53025
Health Effect - Clinical Code No Known Impact Or Consequence To Patient (2692)
Date of Event 05/28/2015
Type of Reportable Event Malfunction
Additional Manufacturer Narrative
This mdr is being filed after the associated complaint was reviewed under remediation protocol (b)(4), complaint/mdr retrospective review and remediation and reassessed as reportable.Additional complaint investigation and record remediation was not performed.
 
Event or Problem Description
It was reported that the balloon of the coda balloon catheter would not deflate after being inflated inside a stent graft for an aortic aneurysm repair procedure.There were no injuries or additional procedures reported.
 
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Brand Name
CODA BALLOON CATHETER
Common Device Name
DQY CATHETER, PERCUTANEOUS
Manufacturer (Section D)
COOK INC
750 daniels way
bloomington IN 47404
MDR Report Key7589104
Report Number1820334-2018-01777
Device Sequence Number1423084
Product Code DQY
UDI-Device Identifier00827002530256
UDI-Public(01)00827002530256(17)161101(10)4617170
Combination Product (Y/N)N
Initial Reporter StateNJ
Initial Reporter CountryUS
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source company representative
Initial Reporter Occupation Nurse
Type of Report Initial
Report Date (Section B) 06/11/2018
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 NumberG53025
Device Catalogue NumberCODA-2-10.0-35-120-40
Was Device Available for Evaluation? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 06/06/2018
Initial Report FDA Received Date06/11/2018
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Patient Sequence Number1
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