KERLIX STERILE GAUZE BANDAGE ROLLS UNKNOWN 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 2019-06-13 for KERLIX STERILE GAUZE BANDAGE ROLLS UNKNOWN PRODUCT manufactured by Covidien.

MAUDE Entry Details

Report Number1018120-2019-00367
MDR Report Key8697579
Report SourceOTHER
Date Received2019-06-13
Date of Report2019-06-13
Date Mfgr Received2019-05-23
Date Added to Maude2019-06-13
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 Street1430 MARVIN GRIFFIN ROAD, PO B
Manufacturer CityAUGUSTA GA 30906
Manufacturer CountryUS
Manufacturer Postal Code30906
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameKERLIX STERILE GAUZE BANDAGE ROLLS
Generic NameGAUZE/SPONGE,NONRESORBABLE FOR EXTERNAL USE
Product CodeNAB
Date Received2019-06-13
Model NumberUNKNOWN PRODUCT
Catalog NumberUNKNOWN PRODUCT
Lot NumberUNKNOWN
Device Availability*
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer Address1430 MARVIN GRIFFIN ROAD, PO B AUGUSTA GA 30906 US 30906


Patients

Patient NumberTreatmentOutcomeDate
101. Deathisabilit 2019-06-13

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