BD VACUTAINER? URINALYSIS CONCIAL URINE TUBE NO ADDITIVE 364980

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-05-31 for BD VACUTAINER? URINALYSIS CONCIAL URINE TUBE NO ADDITIVE 364980 manufactured by Becton, Dickinson & Co..

Event Text Entries

[109773659] Date device returned to manufacturer is unknown. The date of investigation was used. Bd had not received samples or photos from the customer facility for evaluation; therefore, the investigation was limited. Additionally, bd was unable to determine the specific lot number associated with this complaint. Therefore, a review of the device history record could not be conducted.
Patient Sequence No: 1, Text Type: N, H10


[109773660] It was reported that the bd vacutainer? Urinalysis concial urine tube no additive had erroneous results no serious injury medical intervention.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1917413-2018-02307
MDR Report Key7558829
Date Received2018-05-31
Date of Report2018-05-07
Date of Event2016-06-02
Date Mfgr Received2016-06-02
Date Added to Maude2018-05-31
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 ContactBDX BRETT WILKO
Manufacturer Street9450 SOUTH STATE STREET
Manufacturer CitySANDY UT 84070
Manufacturer CountryUS
Manufacturer Postal84070
Manufacturer Phone8015652845
Manufacturer G1BECTON, DICKINSON & CO.
Manufacturer Street150 SOUTH 1ST AVENUE
Manufacturer CityBROKEN BOW NE 68822
Manufacturer CountryUS
Manufacturer Postal Code68822
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameBD VACUTAINER? URINALYSIS CONCIAL URINE TUBE NO ADDITIVE
Generic NameSPECIMEN TRANSPORT AND STORAGE CONTAINER
Product CodeNNK
Date Received2018-05-31
Catalog Number364980
Lot NumberUNKNOWN
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBECTON, DICKINSON & CO.
Manufacturer Address150 SOUTH 1ST AVENUE BROKEN BOW NE 68822 US 68822


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2018-05-31

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