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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: COOK INC UNIVERSA SOFT URETERAL STENT SET; FAD STENT, URETERAL

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COOK INC UNIVERSA SOFT URETERAL STENT SET; FAD STENT, URETERAL Back to Search Results
Model Number G49945
Health Effect - Clinical Code No Known Impact Or Consequence To Patient (2692)
Date of Event 09/28/2016
Type of Reportable Event Malfunction
Additional Manufacturer Narrative
The patient's age was noted to be (b)(6), but the unit for the age is unknown.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 universa soft ureteral stent broke in half upon an attempt to elongate the device and cut the threads off.This product problem occurred prior to patient contact and there was no reported impact to the patient.
 
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Brand Name
UNIVERSA SOFT URETERAL STENT SET
Common Device Name
FAD STENT, URETERAL
Manufacturer (Section D)
COOK INC
750 daniels way
bloomington IN 47404
MDR Report Key7428274
Report Number1820334-2018-01111
Device Sequence Number1233798
Product Code FAD
UDI-Device Identifier00827002499454
UDI-Public(01)00827002499454(17)181014(10)6285468
Combination Product (Y/N)N
Initial Reporter StateFL
Initial Reporter CountryUS
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source distributor,foreign,other
Initial Reporter Occupation Other
Type of Report Initial
Report Date (Section B) 04/13/2018
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 NumberG49945
Device Catalogue NumberUSH-600
Was Device Available for Evaluation? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 04/09/2018
Initial Report FDA Received Date04/13/2018
Patient Sequence Number1
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