MAUDE Adverse Event Report: COLOPLAST A/S (2BO)RESTORELLE DIRECTFIX POS; SURGICAL MESH

Model Number 5014601400

Device Problem Device Operates Differently Than Expected (2913)

Patient Problem Abnormal Vaginal Discharge (2123)

Event Date 10/11/2016

Event Type  Injury  

Manufacturer Narrative

Without the benefit of examination and testing, coloplast is precluded from commenting on the condition of the device or the cause of the occurrence, should additional facts prompt us to alter or supplement any information of conclusions contained in the original mdr or in any prior supplemental reports, a follow-up report will be submitted.

Event Description

As reported to coloplast, though not verified, subject experienced purulent vaginal discharge on (b)(6) 2016 resulting in inpatient hospitalization and surgical procedure on (b)(6) 2016.During procedure, the restorelle df posterior device was partially explanted at the posterior vaginal wall and apex.

• Brand Name: (2BO)RESTORELLE DIRECTFIX POS
• Type of Device: SURGICAL 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 Key: 6025957
• MDR Text Key: 57296066
• Report Number: 2125050-2016-00297
• Device Sequence Number: 1
• Product Code: FTL
• Combination Product (y/n): N
• PMA/PMN Number: K103568
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: consumer,other
• Type of Report: Initial
• Report Date: 10/13/2016

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 10/13/2016
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Physician
• Device Model Number: 5014601400
• Device Catalogue Number: 5014601400
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 10/12/2016
• 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: N
• Patient Sequence Number: 1
• Patient Outcome(s): Other