TOROSA SALINE TESTICULAR LARGE 5206502400

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2018-05-18 for TOROSA SALINE TESTICULAR LARGE 5206502400 manufactured by Coloplast A/s.

Event Text Entries

[108632434] 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 or conclusions contained in the original mdr or in any prior supplemental reports, a follow-up report will be submitted
Patient Sequence No: 1, Text Type: N, H10


[108632435] According to the available information, patient had a testicular implant that had to be removed due to the patient having an allergic reaction after the surgery. The patient will be tested by an allergist.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2125050-2018-00387
MDR Report Key7525684
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2018-05-18
Date of Report2018-07-10
Date of Event2017-12-21
Date Mfgr Received2018-04-25
Date Added to Maude2018-05-18
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 ContactSTEPHANIE PERRYMAN
Manufacturer Street1601 WEST RIVIER ROAD NORTH
Manufacturer CityMINNEAPOLIS MN 55411
Manufacturer CountryUS
Manufacturer Postal55411
Manufacturer Phone6124345685
Manufacturer G1COLOPLAST MANUFACTURING US, LLC
Manufacturer Street1601 WEST RIVIER 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 SALINE TESTICULAR LARGE
Generic NameSALINE FILLED TESTICULAR PROSTHESIS
Product CodeFAF
Date Received2018-05-18
Model Number5206502400
Catalog Number5206502400
Lot Number5713110
OperatorLAY USER/PATIENT
Device AvailabilityN
Device AgeDA
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 2018-05-18

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