UPSYLON? Y MESH KIT M0068318220

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04,07 report with the FDA on 2014-06-04 for UPSYLON? Y MESH KIT M0068318220 manufactured by Boston Scientific - Marlborough.

Event Text Entries

[17611804] As reported by the patient? S attorney, a boston scientific device was implanted. According to the complainant, the patient experienced an unknown injury. All other information is unknown. Should additional relevant details become available, a supplemental report will be submitted.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005099803-2014-02142
MDR Report Key3849681
Report Source04,07
Date Received2014-06-04
Date of Report2014-05-22
Date Mfgr Received2014-05-22
Date Added to Maude2014-06-04
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 FDA0
Event Location0
Manufacturer ContactEMP. INGRID MATTE
Manufacturer Street100 BOSTON SCIENTIFIC WAY
Manufacturer CityMARLBOROUGH MA 01752
Manufacturer CountryUS
Manufacturer Postal01752
Manufacturer Phone5086834000
Manufacturer G1PROXY BIOMEDICAL LIMITED
Manufacturer StreetCOILLEACH SPIDDAL
Manufacturer CityGALWAY
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameUPSYLON? Y MESH KIT
Generic NameGYNECOLOGIC LAPAROSCOPE AND ACCESSORIES
Product CodeOHD
Date Received2014-06-04
Model NumberM0068318220
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBOSTON SCIENTIFIC - MARLBOROUGH
Manufacturer Address100 BOSTON SCIENTIFIC WAY MARLBOROUGH MA 01752 US 01752


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2014-06-04

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.