BD? BLUNT FILL NEEDLE WITH FILTER 305211

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,other,user facility report with the FDA on 2020-03-17 for BD? BLUNT FILL NEEDLE WITH FILTER 305211 manufactured by Bd Medical (bd West) Medical Surgical.

Event Text Entries

[186327764] A device evaluation is anticipated, but has not yet begun. Upon completion of the investigation, a supplemental report will be filed.
Patient Sequence No: 1, Text Type: N, H10


[186327765] It was reported that the tip of the bd? Blunt fill needle with filter fractured and broke off prior to use. The following information was provided by the initial reporter: "tip of needle had fractured and broken off prior to use. "
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1911916-2020-00258
MDR Report Key9843113
Report SourceFOREIGN,OTHER,USER FACILITY
Date Received2020-03-17
Date of Report2020-03-23
Date of Event2019-12-13
Date Mfgr Received2020-02-24
Device Manufacturer Date2019-04-03
Date Added to Maude2020-03-17
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 G1BD MEDICAL (BD WEST) MEDICAL SURGICAL
Manufacturer Street1852 10TH AVENUE
Manufacturer CityCOLUMBUS NE 68601
Manufacturer CountryUS
Manufacturer Postal Code68601
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBD? BLUNT FILL NEEDLE WITH FILTER
Generic NameMANUAL SURGICAL INSTRUMENT FOR GENERAL USE
Product CodeGAA
Date Received2020-03-17
Catalog Number305211
Lot Number9093554
Device Availability*
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBD MEDICAL (BD WEST) MEDICAL SURGICAL
Manufacturer Address1852 10TH AVENUE COLUMBUS NE 68601 US 68601


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-03-17

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