TOROSA 5206501400

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04,07 report with the FDA on 2011-12-06 for TOROSA 5206501400 manufactured by Coloplast A/s.

Event Text Entries

[2504473] Testicular/scrotal pain, implant too hard. Device remains implanted.
Patient Sequence No: 1, Text Type: D, B5


[9567972] Device remains implanted; therefore no device evaluation was performed. Without the benefit of examination and testing, coloplast cannot confirm the complaint or the cause of the occurrence. Device still implanted.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2125050-2011-00015
MDR Report Key2360283
Report Source04,07
Date Received2011-12-06
Date of Report2011-11-08
Date Mfgr Received2011-11-08
Date Added to Maude2011-12-07
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 FDA3
Report to FDA0
Event Location0
Manufacturer ContactTIM CRABTREE-RA MANAGER
Manufacturer Street1601 W. RIVER ROAD N
Manufacturer CityMINNEAPOLIS MN 55411
Manufacturer CountryUS
Manufacturer Postal55411
Manufacturer Phone6123024922
Manufacturer G1COLOPLAST MANUFACTURING US, LLC
Manufacturer Street1601 W. RIVER ROAD N
Manufacturer CityMINNEAPOLIS MN 55411
Manufacturer CountryUS
Manufacturer Postal Code55411
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTOROSA
Generic NameSALINE FILLED TESTICULAR PROSTHESIS
Product CodeFAF
Date Received2011-12-06
Model Number5206501400
Catalog Number5206501400
Lot NumberUNKNOWN
OperatorLAY USER/PATIENT
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. Required No Informationntervention 2011-12-06

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