BD? SYRINGE 3ML HEPARIN 10 UNIT 306413

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-02-13 for BD? SYRINGE 3ML HEPARIN 10 UNIT 306413 manufactured by Bd Medical (bd West) Medical Surgical.

Event Text Entries

[100065462] Date of event: unknown. The date received by manufacturer has been used for this field. The customer's address is unknown. (b)(6), usa has been used as a default. A device evaluation is anticipated, but has not yet begun. Upon completion of the investigation and/or device history review, a supplemental report will be filed.
Patient Sequence No: 1, Text Type: N, H10


[100065463] It was reported that multiple times, the plunger of a bd? Syringe 3ml heparin 10 unit will? Come out? While drawing up medication. There was no report of exposure, injury or medical intervention.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1911916-2018-00062
MDR Report Key7268220
Date Received2018-02-13
Date of Report2018-03-14
Date of Event2017-11-28
Date Mfgr Received2017-11-28
Device Manufacturer Date2017-04-21
Date Added to Maude2018-02-13
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationPATIENT
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 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 Report0

Device Details

Brand NameBD? SYRINGE 3ML HEPARIN 10 UNIT
Generic NameHEPARIN FLUSH
Product CodeNZW
Date Received2018-02-13
Catalog Number306413
Lot Number711169N
Device Expiration Date2018-10-31
OperatorLAY USER/PATIENT
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 2018-02-13

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