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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: COLOPLAST A/S (2BO) RESTORELLE DIRECT FIX A SURGICAL MESH

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COLOPLAST A/S (2BO) RESTORELLE DIRECT FIX A SURGICAL MESH Back to Search Results
Model Number 5013601400
Device Problem Device Operates Differently Than Expected (2913)
Patient Problem Abnormal Vaginal Discharge (2123)
Event Date 03/07/2014
Event Type  Injury  
Manufacturer Narrative

Coloplast has not been provided any corroborating evidence to verify the information contained in this report.

 
Event Description

As reported to coloplast, though not verified,patient's legal representative stated mesh exposure near bladder neck, bard dingle incision sling placed at the same time as restorelle a, unlikely related to restorelle a, vaginal discharge, spotting, and mesh exposure on left vagina.

 
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Brand Name(2BO) RESTORELLE DIRECT FIX A
Type of DeviceSURGICAL MESH
Manufacturer (Section D)
COLOPLAST A/S
holtedam 1
humlebaek, da 3050
DA 3050
Manufacturer (Section G)
COLOPLAST MANUFACTURING US, LLC
1601 west river road north
minneapolis MN 55411
Manufacturer Contact
christine buckvold
1601 west river road north
minneapolis, MN 55411
6123024982
MDR Report Key6171481
MDR Text Key62311299
Report Number2125050-2016-00380
Device Sequence Number1
Product Code FTL
Combination Product (Y/N)N
PMA/PMN NumberK103568
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type CONSUMER,OTHER
Type of Report Initial
Report Date 12/13/2016
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received12/13/2016
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator
Device MODEL Number5013601400
Device Catalogue Number5013601400
Was Device Available For Evaluation? No
Was the Report Sent to FDA?
Event Location No Information
Date Manufacturer Received12/07/2016
Was Device Evaluated By Manufacturer? Device Not Returned To Manufacturer
Is The Device Single Use? Yes
Is this a Reprocessed and Reused Single-Use Device? No
Type of Device Usage

Patient TREATMENT DATA
Date Received: 12/13/2016 Patient Sequence Number: 1
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