FENIX CONTINENCE RESTRORATION SYSTEM FS15 NA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2016-03-15 for FENIX CONTINENCE RESTRORATION SYSTEM FS15 NA manufactured by Torax Medical, Inc..

Event Text Entries

[40346192] Following a surgical procedure for reinforcement of the anal sphincter due to fecal incontinence, a patient experienced rectal pain and erosion of the fenix device with infection leading to fenix device explant. The fenix device was used as part of the surgical procedure. Uneventful surgical procedure and device implant on (b)(6) 2014. Due to lack of fecal incontinence improvement, a neurotransmitter was used on the patient while still implanted with fenix in (b)(6) 2015. Uneventful device explant (b)(6) 2015 due to pain after bowel movement with subsequent discovery of an erosion with infection of the fenix device. The fenix device was intact.
Patient Sequence No: 1, Text Type: D, B5


[69767320] Added (b)(4) so as to be consistent with information. Updated product code from mip to pmh.
Patient Sequence No: 1, Text Type: N, H10


[69767321] Following a surgical procedure for reinforcement of the anal sphincter due to fecal incontinence, a patient experienced rectal pain and erosion of the fenix device with infection leading to fenix device explant. The fenix device was used as part of the surgical procedure. Uneventful surgical procedure and device implant on (b)(6) 2014. Due to lack of fecal incontinence improvement, a neurotransmitter was used on the patient while still implanted with fenix in (b)(6) 2015. Uneventful device explant (b)(6) 2015 due to pain after bowel movement with subsequent discovery of an erosion with infection of the fenix device. The fenix device was intact.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3008766073-2016-00018
MDR Report Key5501002
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2016-03-15
Date of Report2017-03-07
Date of Event2015-12-16
Date Mfgr Received2017-03-07
Device Manufacturer Date2012-08-13
Date Added to Maude2016-03-15
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. DANIEL HOSECK
Manufacturer Street4188 LEXINGTON AVENUE NORTH
Manufacturer CitySHOREVIEW MN 55126
Manufacturer CountryUS
Manufacturer Postal55126
Manufacturer Phone6513618900
Manufacturer G1TORAX MEDICAL, INC.
Manufacturer Street4188 LEXINGTON AVENUE NORTH
Manufacturer CitySHOREVIEW MN 55126
Manufacturer CountryUS
Manufacturer Postal Code55126
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Sequence Number: 0

Brand NameFENIX CONTINENCE RESTRORATION SYSTEM
Generic NameIMPLANTED FECAL INCONTINENCE DEVICE
Product CodePMH
Date Received2016-03-15
Model NumberFS15
Catalog NumberNA
Lot Number3867
Device Expiration Date2016-08-13
OperatorPHYSICIAN
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No0
Device Event Key0
ManufacturerTORAX MEDICAL, INC.
Manufacturer Address4188 LEXINGTON AVENUE N SHOREVIEW MN 55126 US 55126

Device Sequence Number: 1

Brand NameFENIX CONTINENCE RESTRORATION SYSTEM
Generic NameIMPLANTED FECAL INCONTINENCE DEVICE
Product CodePMH
Date Received2016-03-15
Model NumberFS15
Catalog NumberNA
Lot Number3867
Device Expiration Date2016-08-13
OperatorPHYSICIAN
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerTORAX MEDICAL, INC.
Manufacturer Address4188 LEXINGTON AVENUE N SHOREVIEW MN 55126 US 55126


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Deathisabilit 2016-03-15

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