CONTAINER SHARPS 5QT RED 8507SA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2019-08-30 for CONTAINER SHARPS 5QT RED 8507SA manufactured by Covidien.

MAUDE Entry Details

Report Number1424643-2019-00544
MDR Report Key8950522
Report SourceCOMPANY REPRESENTATIVE,USER F
Date Received2019-08-30
Date of Report2019-08-30
Date of Event2019-08-16
Date Mfgr Received2019-08-16
Date Added to Maude2019-08-30
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 ContactJILL SARAIVA
Manufacturer Street15 HAMPSHIRE STREET
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal02048
Manufacturer Phone5086183640
Manufacturer G1COVIDIEN
Manufacturer Street815 TEK DRIVE
Manufacturer CityCRYSTAL LAKE IL 600399002
Manufacturer CountryUS
Manufacturer Postal Code600399002
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCONTAINER SHARPS 5QT RED
Generic NameCONTAINER, SHARPS
Product CodeMMK
Date Received2019-08-30
Model Number8507SA
Catalog Number8507SA
Lot Number19D05763
Device Availability*
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer Address815 TEK DRIVE CRYSTAL LAKE IL 600399002 US 600399002


Patients

Patient NumberTreatmentOutcomeDate
10 2019-08-30

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