PN 32GX4MM ENGLISH 320137

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer,foreign,other report with the FDA on 2020-03-19 for PN 32GX4MM ENGLISH 320137 manufactured by Becton Dickinson And Co..

Event Text Entries

[186307381] Date of event: unknown. The date received by manufacturer has been used for this field. A device evaluation and/or device history review is anticipated, but is not complete. Upon completion, a supplemental report will be filed.
Patient Sequence No: 1, Text Type: N, H10


[186307382] It was reported that pn 32gx4mm english was clogged during injection. The following information was provided by the initial reporter: details of complaint: customer was injecting require amount of insulin when needle stopped working during the injection process (only delivered 3 units of insulin).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9616656-2020-00241
MDR Report Key9853403
Report SourceCONSUMER,FOREIGN,OTHER
Date Received2020-03-19
Date of Report2020-03-25
Date of Event2020-02-28
Date Mfgr Received2020-02-28
Device Manufacturer Date2019-08-28
Date Added to Maude2020-03-19
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 CO.
Manufacturer StreetPOTTERY ROAD
Manufacturer CityDUN LAOGHAIRE CO
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePN 32GX4MM ENGLISH
Generic NamePEN NEEDLE
Product CodeFMI
Date Received2020-03-19
Catalog Number320137
Lot Number9240198
OperatorLAY USER/PATIENT
Device Availability*
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBECTON DICKINSON AND CO.
Manufacturer AddressPOTTERY ROAD DUN LAOGHAIRE CO


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-03-19

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