UNKNOWN PROGRIP MESH PRODUCT

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 2020-03-31 for UNKNOWN PROGRIP MESH PRODUCT manufactured by Sofradim Production Sas.

Event Text Entries

[185947547] If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[185947548] According to the reporter, seven years after an inguinal hernia procedure, the patient was having discomfort and on and off extreme, debilitating pain from the mesh that was implanted in him.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9615742-2020-00763
MDR Report Key9903468
Report SourceOTHER
Date Received2020-03-31
Date of Report2020-03-31
Date Mfgr Received2020-03-04
Date Added to Maude2020-03-31
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 ContactLISA HERNANDEZ
Manufacturer Street60 MIDDLETOWN AVE.
Manufacturer CityNORTH HAVEN CT 06473
Manufacturer CountryUS
Manufacturer Postal06473
Manufacturer Phone2034925563
Manufacturer G1SOFRADIM PRODUCTION SAS
Manufacturer Street116 AVENUE DU FORMANS
Manufacturer CityTREVOUX 01600
Manufacturer CountryFR
Manufacturer Postal Code01600
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameUNKNOWN PROGRIP MESH PRODUCT
Generic NameMESH, SURGICAL, POLYMERIC
Product CodeFTL
Date Received2020-03-31
Model NumberUNKNOWN PROGRIP MESH PRODUCT
Catalog NumberUNKNOWN PROGRIP MESH PRODUCT
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerSOFRADIM PRODUCTION SAS
Manufacturer Address116 AVENUE DU FORMANS TREVOUX 01600 FR 01600


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-03-31

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