BD - VACUTAINER PUSH BUTTON BLOOD COLLECTION SET

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-03-10 for BD - VACUTAINER PUSH BUTTON BLOOD COLLECTION SET manufactured by Becton Dickinson And Company.

Event Text Entries

[17204978] On (b)(6) 2015, the phlebotomist use the bd vacutainer push button blood collection set (butterfly needle) (b)(4) - 23g x 3/4" x 12" for a patient. She did a veinpuncture and after difficulty on her first try, she noticed the needle to be bent at the tip like a hook. She replaced it with a new butterfly needle.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5041483
MDR Report Key4611828
Date Received2015-03-10
Date of Report2015-03-10
Date of Event2015-03-01
Date Added to Maude2015-03-19
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional0
Initial Report to FDA3
Report to FDA0
Event Location0
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameBD - VACUTAINER PUSH BUTTON BLOOD COLLECTION SET
Generic NameBD - VACUTAINER PUSH BUTTON BLOOD COLLECTION SET
Product CodeKST
Date Received2015-03-10
Lot Number#4247827
ID NumberREF: 367342
Device Expiration Date2016-08-01
OperatorHEALTH PROFESSIONAL
Device Sequence No1
Device Event Key0
ManufacturerBECTON DICKINSON AND COMPANY


Patients

Patient NumberTreatmentOutcomeDate
10 2015-03-10

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