FDA Adverse Event Malfunction Summary report: N

BD¿ 5ML SYRINGE

MDR report key: 7035851 · Received November 15, 2017

Report

Report Number
3002682307-2017-00094
Event Type
Malfunction
Date Received
November 15, 2017
Date of Event
October 24, 2017
Report Date
October 30, 2017
Manufacturer
BECTON DICKINSON, S.A.
Product Code
FMF
PMA / PMN Number
N/A
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

RESULTS: SAMPLE EVALUATION: WE HAVE BEEN PROVIDED WITH THE AFFECTED SAMPLES. A LEAKAGE THROUGH THE PLUNGER ROD WAS OBSERVED IN THIS PROVIDED SAMPLES. WE COULD NOT DETERMINATE THE EXACT ROOT CAUSE DUE TO THE PRESENCE OF DRY BLOOD INSIDE THE SYRINGES. THE SAMPLES WERE NOT DECONTAMINATED. BHR REVIEW: WE HAVE REVIEWED OUR PRODUCTION AND INSPECTION RECORDS AND HAVE ESTABLISHED THAT ALL PRODUCTION AND QUALITY PROCESSES WERE CARRIED OUT NORMALLY FOR LOTS 7114310, 7100033, 7089480, 7114314, 71100038, 7089481, AND 7083117 AND NO PROBLEMS, DEFECTS OR QN RELATED TO THE REPORTED ISSUE WERE FOUND. ROOT CAUSE ANALYSIS: WE CONCLUDE THAT THE CAUSE OF THE PROBLEM COULD BE PRODUCED AS A CONSEQUENCE OF A DAMAGE IN THE PLUNGER LIP. THIS COULD BE PRODUCED DURING THE HANDLING OF THE PRODUCT THROUGH THE MANUFACTURING PROCESS OR IN THE PLUNGER ASSEMBLY MACHINE. CONFIRMATION: THE PROVIDED SAMPLE PRESENTED THE REPORTED ISSUE. WE COULD CONFIRM THE REPORTED ISSUE. CAPA DETERMINATION: BASED ON AN EVALUATION OF SEVERITY AND OCCURRENCE IT WAS DETERMINATE THAT NO CORRECTIVE ACTION IS REQUIRED AT THIS TIME.

Description of Event or Problem · 1

IT WAS REPORTED THAT A NURSE FOUND BLOOD LEAKING FROM THE PLUNGER OF A BD¿ 5 ML SYRINGE WHILE DRAWING BLOOD. THERE WAS NO REPORT OF INJURY OR MEDICAL INTERVENTION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
814523 BD¿ 5ML SYRINGE SYRINGE FMF BECTON DICKINSON, S.A. 1704180

Patients

Seq Age Sex Outcome Treatment
1 Other