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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: COOK INC HIGH PRESSURE BRAIDED CONNECTING TUBE

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COOK INC HIGH PRESSURE BRAIDED CONNECTING TUBE Back to Search Results
Model Number G00069
Health Effect - Clinical Code No Information (3190)
Date of Event 07/08/2015
Type of Reportable Event Malfunction
Additional Manufacturer Narrative
Common name: dtl adaptor, stopcock, manifold, fitting, cardiopulmonary bypass.Product code: dtl.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 when the procedure started, a leakage was found at the high pressure braided connector of the tube which was attached to the injector.The patient did not experience any adverse effects due to this occurrence.
 
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Brand Name
HIGH PRESSURE BRAIDED CONNECTING TUBE
Manufacturer (Section D)
COOK INC
750 daniels way
bloomington IN 47404
MDR Report Key7476808
Report Number1820334-2018-01342
Device Sequence Number11117190
Product Code GAZ
UDI-Device Identifier00827002000698
UDI-Public(01)00827002000698(17)180403(10)5776355
Combination Product (Y/N)N
Initial Reporter CountryTW
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source company representative,foreig
Initial Reporter Occupation Physician
Type of Report Initial
Report Date (Section B) 05/01/2018
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 NumberG00069
Device Catalogue NumberHPCT8.8-80-P-FM
Was Device Available for Evaluation? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 04/30/2018
Initial Report FDA Received Date05/01/2018
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Patient Sequence Number1
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