GYNECARE GYNEMSH PS 4INX6IN GPSL

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other report with the FDA on 2020-02-06 for GYNECARE GYNEMSH PS 4INX6IN GPSL manufactured by Ethicon Inc..

Event Text Entries

[177989823] (b)(4). To date, the device has not been returned. If the product is returned for evaluation, any further information derived from the evaluation will be submitted in a supplemental 3500a form.
Patient Sequence No: 1, Text Type: N, H10


[177989824] It was reported by an attorney that the patient underwent a gynecological surgical procedure on (b)(6) 2004 and mesh was implanted. It was reported that she experienced pelvic pain, vaginal bleeding, pain during intercourse, urinary incontinence and frequent urinary tract infections. It was reported that on (b)(6) 2016 and (b)(6) 2018, the patient was noted to have mesh erosion through her vagina. No additional information was provided.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2210968-2020-00975
MDR Report Key9676925
Report SourceOTHER
Date Received2020-02-06
Date of Report2020-02-05
Date Mfgr Received2020-02-05
Date Added to Maude2020-02-06
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 INC.-SAN LORENZO PR
Manufacturer Street982 ROAD 183 KM 8.3
Manufacturer CitySAN LORENZO PR
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameGYNECARE GYNEMSH PS 4INX6IN
Generic NameMESH, SURGICAL, SYNTHETIC, UROGYNECOLOGIC
Product CodeOTO
Date Received2020-02-06
Model NumberGPSL
Catalog NumberGPSL
Lot NumberUNK
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
10 2020-02-06

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