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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: COOK INC TRIPLE LUMEN HEPARIN COATED CENTRAL VENOUS CATHETER TRAY; DQY CATHETER, PERCUTANEOUS

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COOK INC TRIPLE LUMEN HEPARIN COATED CENTRAL VENOUS CATHETER TRAY; DQY CATHETER, PERCUTANEOUS Back to Search Results
Catalog Number C-UTLMY-501J-RSC-BH
Health Effect - Clinical Code No Known Impact Or Consequence To Patient (2692)
Date of Event 03/08/2016
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 the dilator could not be advanced through the catheter as the dilator tip was damaged and frayed.As a result, the procedure was completed with a different dilator.
 
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Brand Name
TRIPLE LUMEN HEPARIN COATED CENTRAL VENOUS CATHETER TRAY
Common Device Name
DQY CATHETER, PERCUTANEOUS
Manufacturer (Section D)
COOK INC
750 daniels way
bloomington IN 47404
MDR Report Key6892038
Report Number1820334-2017-03329
Device Sequence Number16302999
Product Code DQY
UDI-Device Identifier00827002045422
UDI-Public(01)00827002045422(17)180228(10)NS6145023
Combination Product (Y/N)N
Initial Reporter StateTX
Initial Reporter CountryUS
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source user facility
Initial Reporter Occupation Other
Type of Report Initial
Report Date (Section B) 09/25/2017
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 Catalogue NumberC-UTLMY-501J-RSC-BH
Was Device Available for Evaluation? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 09/12/2017
Initial Report FDA Received Date09/25/2017
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Patient Sequence Number1
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