FDA Adverse Event No answer provided Summary report: N

BD VACUTAINER K2 EDTA 3.6 MG

MDR report key: 15657348 · Received October 24, 2022

Report

Report Number
15657348
Event Type
No answer provided
Date Received
October 24, 2022
Date of Event
August 16, 2021
Report Date
September 20, 2022
Manufacturer
BECTON, DICKINSON AND COMPANY
Product Code
JKA
Report Source
User Facility report
Reporter Location
MA
Reporter Occupation
NURSE
Health Professional
Yes

Narratives

Description of Event or Problem · 0

ITEM IS BACKORDERED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2805540 BD VACUTAINER K2 EDTA 3.6 MG TUBES, VIALS, SYSTEMS, SERUM SEPARATORS, BLOOD COLLECTION JKA BECTON, DICKINSON AND COMPANY 367841

Patients

Seq Age Sex Outcome Treatment
1 Unknown