FDA Adverse Event Malfunction Summary report: N

BECTON, DICKINSON AND COMPANY

MDR report key: 9947869 · Received April 10, 2020

Report

Report Number
9947869
Event Type
Malfunction
Date Received
April 10, 2020
Date of Event
February 13, 2020
Report Date
March 24, 2020
Manufacturer
BECTON, DICKINSON AND COMPANY
Product Code
FMF
Product Problem
Yes
Report Source
User Facility report
Reporter Location
AZ
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

REPORT BEING ENTERED FOR TRACKING PURPOSES ONLY-DO NOT HAVE SERIAL OR MODEL NUMBERS. NYICU (NURSERY INTENSIVE CARE UNIT) RN NOTED LEAKING AT 3CC SYRINGE BUFF CAP DURING AN IV HYDROCORTISONE ADMINISTRATION. PHARMACY IS WORKING TO BRING IN A DIFFERENT COMPANY FOR 3CC SYRINGES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
412052 BECTON, DICKINSON AND COMPANY SYRINGE, PISTON FMF BECTON, DICKINSON AND COMPANY

Patients

Seq Age Sex Outcome Treatment
1