VIRTUE MALE SLING SYSTEM

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other report with the FDA on 2020-03-19 for VIRTUE MALE SLING SYSTEM manufactured by Coloplast A/s.

Event Text Entries

[186103670] Coloplast has not been provided any corroborating evidence to verify the information contained in this report. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[186103671] As reported to coloplast though not verified, legal representative stated the patient suffered bodily injuries, including but not limited to, foreign body reaction, mesh protrusion, mesh erosion into the urethra requiring surgical removal, pelvic pain, bowel problems, urinary problems, testicular pain, scrotal sac pain and other injuries.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2125050-2020-00260
MDR Report Key9857363
Report SourceOTHER
Date Received2020-03-19
Date of Report2020-03-19
Date Mfgr Received2020-02-20
Date Added to Maude2020-03-19
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer ContactSARAH O'GARA
Manufacturer Street1601 WEST RIVER ROAD NORTH
Manufacturer CityMINNEAPOLIS, MN
Manufacturer CountryUS
Manufacturer G1COLOPLAST MANUFACTURING US, LLC
Manufacturer Street1601 WEST RIVER ROAD NORTH
Manufacturer CityMINNEAPOLIS, MN
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVIRTUE MALE SLING SYSTEM
Generic NameSURGICAL MESH
Product CodeOTM
Date Received2020-03-19
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCOLOPLAST A/S
Manufacturer AddressHOLTEDAM 1 HUMLEBAEK, 3050 DA 3050


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-03-19

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