FDA Adverse Event Injury Summary report: N

BECTON DICKINSON

MDR report key: 1998796 · Received February 15, 2011

Report

Report Number
MW5019448
Event Type
Injury
Date Received
February 15, 2011
Date of Event
January 28, 2011
Report Date
February 15, 2011
Manufacturer
BECTON DICKINSON AND CO., BECTON DICKINSON
Product Code
FMI
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
TX, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

BD 30G 1" PRECISION BROKE OFF OF SYRINGE INSIDE PT AFTER 5TH PASS OF LIDOCAINE INJECTIONS ON (B)(6) 2011.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BECTON DICKINSON NEEDLE HYPODERMIC FMI BECTON DICKINSON AND CO., BECTON DICKINSON 0210910

Patients

Seq Age Sex Outcome Treatment
1 Disability