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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: COLOPLAST A/S HYDRO X-FLOW CATHETER SILICONE WITH HYDROGEL COATING; INDWELLING URETHRAL DRAINAGE BALLOON CATHETER, NON-ANTIMICROBIAL

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COLOPLAST A/S HYDRO X-FLOW CATHETER SILICONE WITH HYDROGEL COATING; INDWELLING URETHRAL DRAINAGE BALLOON CATHETER, NON-ANTIMICROBIAL Back to Search Results
Catalog Number XB6320
Device Problem Complete Blockage (1094)
Patient Problem Fluid Discharge (2686)
Event Date 11/22/2023
Event Type  malfunction  
Event Description
According to the available information the catheter appeared to be clogged.The urine flowed into the meatus and not into the tube and had leakage of urine and ineffectiveness of the catheter.The catheter was changed successfully.
 
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Brand Name
HYDRO X-FLOW CATHETER SILICONE WITH HYDROGEL COATING
Type of Device
INDWELLING URETHRAL DRAINAGE BALLOON CATHETER, NON-ANTIMICROBIAL
Manufacturer (Section D)
COLOPLAST A/S
1 holtedam humlebaek, dk 3050
humlebaek 3050
DA  3050
Manufacturer (Section G)
CMF-SARLAT
9 avenue edmond rostand
sarlat-la-caneda
FR  
Manufacturer Contact
usbes brian schmidt
1601 west river road n
minneapolis, MN 55411
MDR Report Key18445530
MDR Text Key331916940
Report Number9610711-2024-00005
Device Sequence Number1
Product Code EZL
UDI-Device Identifier03600040260821
UDI-Public3600040260821
Combination Product (y/n)N
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Foreign,Health Professional
Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date 01/04/2024
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
Device Operator Health Professional
Device Catalogue NumberXB6320
Device Lot Number7968964_XB63201002
Is the Reporter a Health Professional? Yes
Initial Date Manufacturer Received Not provided
Initial Date FDA Received01/04/2024
Date Device Manufactured04/21/2021
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
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