PAXGENE? BLOOD DNA TUBE 761165

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other,user facility report with the FDA on 2020-03-16 for PAXGENE? BLOOD DNA TUBE 761165 manufactured by Becton, Dickinson And Company (bd).

Event Text Entries

[186304747] Medical device lot #: unknown. Medical device expiration date: unknown. A device evaluation is anticipated, but has not yet begun. Upon completion of the investigation, a supplemental report will be filed. Device manufacture date: unknown.
Patient Sequence No: 1, Text Type: N, H10


[186304748] It was reported after use the paxgene? Blood dna tube had erroneous results. The following information was provided by the initial reporter: "the blood is fractionation, customer inverts 10 time after collection and then lets it sit for 72 hour then inverts the blood 8-10 time before freezing.?
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9617032-2020-00249
MDR Report Key9837186
Report SourceOTHER,USER FACILITY
Date Received2020-03-16
Date of Report2020-03-18
Date of Event2020-02-24
Date Mfgr Received2020-02-24
Date Added to Maude2020-03-16
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 (BD)
Manufacturer StreetBELLIVER WAY BELLIVER INDUSTRIAL ESTATE
Manufacturer CityPLYMOUTH
Manufacturer CountryUK
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePAXGENE? BLOOD DNA TUBE
Generic NameBLOOD SPECIMEN COLLECTION DEVICE
Product CodePJE
Date Received2020-03-16
Model Number761165
Catalog Number761165
Lot NumberUNKNOWN
Device Availability*
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBECTON, DICKINSON AND COMPANY (BD)
Manufacturer AddressBELLIVER WAY BELLIVER INDUSTRIAL ESTATE PLYMOUTH UK


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-03-16

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