TITAN TOUCH INFR ZERO ANG 16CM ES28162400 ES2816

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 2020-01-15 for TITAN TOUCH INFR ZERO ANG 16CM ES28162400 ES2816 manufactured by Coloplast A/s.

Event Text Entries

[175204705] The lot number was reviewed for complaint trend, nonconforming reports and capa review. No trends were noted. The device has been received at coloplast; however the evaluation is not yet complete. Without the benefit of examination and testing, coloplast is precluded from commenting on the condition of the device or the cause of the occurrence. Once our evaluation is complete, a follow-up report will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[175204706] According to the available information, a pump malfunction was reported. Another inflatable penile prosthesis was implanted.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2125050-2020-00040
MDR Report Key9593407
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-01-15
Date of Report2020-01-15
Date of Event2019-12-16
Date Mfgr Received2019-12-16
Date Added to Maude2020-01-15
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 55411
Manufacturer CountryUS
Manufacturer Postal55411
Manufacturer Phone6123578517
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 NameTITAN TOUCH INFR ZERO ANG 16CM
Generic NameINFLATABLE PENILE PROSTHESIS
Product CodePAH
Date Received2020-01-15
Returned To Mfg2019-12-26
Model NumberES28162400
Catalog NumberES2816
Lot Number5169616
OperatorLAY USER/PATIENT
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCOLOPLAST A/S
Manufacturer AddressHOLTEDAM 1 HUMLEBAEK, 3050 DA 3050


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-01-15

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