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 2020-03-03 for GYNECARE GYNEMSH PS 4INX6IN GPSL manufactured by Ethicon Inc..

Event Text Entries

[188537923] (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. A review of the batch manufacturing records was conducted and the batch met all finished goods release criteria.
Patient Sequence No: 1, Text Type: N, H10


[188537924] It was reported by an attorney that she underwent a gynecological surgical procedure on (b)(6) 2007 and mesh was implanted, due to her pelvic organ prolapse. It was reported that she underwent revision surgery on (b)(6) 2017. It was reported that she experienced undisclosed adverse event. No additional information was provided.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2210968-2020-01300
MDR Report Key9779476
Report SourceOTHER
Date Received2020-03-03
Date of Report2020-02-19
Date Mfgr Received2020-02-18
Device Manufacturer Date2007-07-19
Date Added to Maude2020-03-03
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 00754
Manufacturer Country*
Manufacturer Postal Code00754
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 Received2020-03-03
Model NumberGPSL
Catalog NumberGPSL
Lot NumberZHE932
Device Expiration Date2012-07-31
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 2020-03-03

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