SILCON THORACIC CATH 32FR 8888572560

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-11 for SILCON THORACIC CATH 32FR 8888572560 manufactured by Covidien.

MAUDE Entry Details

Report Number1282497-2019-08554
MDR Report Key8781283
Date Received2019-07-11
Date of Report2019-11-18
Date of Event2019-06-13
Date Mfgr Received2019-06-18
Date Added to Maude2019-07-11
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 Street15 HAMPSHIRE STREET
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal Code02048
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSILCON THORACIC CATH 32FR
Generic NameCATHETER, VENTRICULAR, GENERAL & PLASTIC SURGERY
Product CodeGBS
Date Received2019-07-11
Model Number8888572560
Catalog Number8888572560
Lot Number183550275
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer Address15 HAMPSHIRE STREET MANSFIELD MA 02048 US 02048


Patients

Patient NumberTreatmentOutcomeDate
10 2019-07-11

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