TVT EXACT RETROPUBIC SYSTEM TVTRL

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,other report with the FDA on 2020-03-27 for TVT EXACT RETROPUBIC SYSTEM TVTRL manufactured by Ethicon Inc..

Event Text Entries

[186687883] (b)(4). To date the device has not been returned yet. If the device or further details are received at the later date a supplemental medwatch will be sent.
Patient Sequence No: 1, Text Type: N, H10


[186687884] It was reported that the patient underwent a sling procedure on (b)(6) 2019 and the mesh was implanted. The patient experienced mesh exposure less than 5 mm with no pain and underwent a partial excision of exposed area on (b)(6) 2020. No further information is available.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2210968-2020-02446
MDR Report Key9892408
Report SourceFOREIGN,OTHER
Date Received2020-03-27
Date of Report2020-03-04
Date of Event2020-03-03
Date Mfgr Received2020-03-04
Device Manufacturer Date2019-03-25
Date Added to Maude2020-03-27
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 ContactKARA DITTY-BOVARD
Manufacturer StreetP.O. BOX 151, ROUTE 22 WEST
Manufacturer CitySOMERVILLE NJ 08876
Manufacturer CountryUS
Manufacturer Postal08876
Manufacturer Phone6107428552
Manufacturer G1ETHICON SARL-NEUCHATEL
Manufacturer StreetPUITS-GODET 20
Manufacturer CityNEUCHATEL
Manufacturer CountrySZ
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTVT EXACT RETROPUBIC SYSTEM
Generic NameMESH, SURGICAL, SYNTHETIC, UROGYNECOLOGIC
Product CodeOTN
Date Received2020-03-27
Model NumberTVTRL
Catalog NumberTVTRL
Lot Number3934155
Device Expiration Date2020-02-29
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerETHICON INC.
Manufacturer AddressP.O. BOX 151, ROUTE 22 WEST SOMERVILLE NJ 08876 US 08876


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-27

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