FDA Adverse Event Malfunction Summary report: N

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MDR report key: 3251522 · Received May 2, 2013

Report

Report Number
3251522
Event Type
Malfunction
Date Received
May 2, 2013
Report Date
March 29, 2013
Manufacturer
*
Product Code
---
Product Problem
Yes
Report Source
User Facility report
Reporter Location
TX, US

Narratives

Description of Event or Problem · 1

A NURSE PULLED A 30 UNIT INSULIN SYRINGE AND OPENED IT AND IT HAD SOME TYPE OF DUSTY FUR ON THE NEEDLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
193642 * * --- *
193805 * SYRINGE FMF BECTON DICKINSON * 2298387

Patients

Seq Age Sex Outcome Treatment
1 *