SYRINGE CATHETER TIP 2OZ 309620

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-08-15 for SYRINGE CATHETER TIP 2OZ 309620 manufactured by Becton Dickinson And Company.

MAUDE Entry Details

Report Number2243072-2019-01726
MDR Report Key8898531
Date Received2019-08-15
Date of Report2019-09-24
Date of Event2019-07-30
Date Mfgr Received2019-07-30
Date Added to Maude2019-08-15
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactBDX BRETT WILKO
Manufacturer Street9450 SOUTH STATE STREET
Manufacturer CitySANDY UT 84070
Manufacturer CountryUS
Manufacturer Postal84070
Manufacturer Phone8015652341
Manufacturer G1BECTON DICKINSON AND COMPANY
Manufacturer Street2153 12TH AVENUE
Manufacturer CityCOLUMBUS NE 68601
Manufacturer CountryUS
Manufacturer Postal Code68601
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameSYRINGE CATHETER TIP 2OZ
Generic NameIRRIGATING SYRINGE
Product CodeKYZ
Date Received2019-08-15
Catalog Number309620
Lot Number8360828
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBECTON DICKINSON AND COMPANY
Manufacturer Address2153 12TH AVENUE COLUMBUS NE 68601 US 68601


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-08-15

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