TOROSA 5206502400

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,07 report with the FDA on 2015-01-09 for TOROSA 5206502400 manufactured by Coloplast A/s.

Event Text Entries

[5121818] As reported to coloplast though not verified, patient was implanted with a coloplast testicular without filling with saline.
Patient Sequence No: 1, Text Type: D, B5


[12642154] Coloplast has not been provided any corroborating evidence to verify the information contained in this report. Device not returned.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2125050-2014-00437
MDR Report Key4403643
Report Source05,07
Date Received2015-01-09
Date of Report2014-12-09
Date of Event2014-12-08
Date Mfgr Received2014-12-09
Date Added to Maude2015-01-09
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactMS. ANGELA KILLIAN - HEAD OF RA
Manufacturer Street1601 WEST RIVER ROAD NORTH
Manufacturer CityMINNEAPOLIS MN 55411
Manufacturer CountryUS
Manufacturer Postal55411
Manufacturer Phone6122874236
Manufacturer G1COLOPLAST MANUFACTURING US LLC
Manufacturer Street1601 WEST RIVER ROAD NORTH
Manufacturer CityMINNEAPOLIS MN 55411
Manufacturer CountryUS
Manufacturer Postal Code55411
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTOROSA
Generic NameTESTICULAR PROSTHESIS
Product CodeFAF
Date Received2015-01-09
Model Number5206502400
Lot Number4047817
Device Expiration Date2019-02-28
OperatorPHYSICIAN
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCOLOPLAST A/S
Manufacturer AddressHOLTEDAM-1 HUMLEBAEK 3050, DK


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2015-01-09

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