FDA Adverse Event Injury Summary report: N

NMT SAFTEY SYRINGE

MDR report key: 507796 · Received January 20, 2004

Report

Report Number
507796
Event Type
Injury
Date Received
January 20, 2004
Date of Event
July 18, 2003
Report Date
January 16, 2004
Manufacturer
NEW MEDICAL TECHNOLOGY, INC.
Product Code
FMF
Adverse Event
Yes
Report Source
User Facility report
Reporter Location
HI, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

ATTEMPTED TO USE PRODUCT, NEEDLE FAILED. STAFF MEMBER GOT A NEEDLESTICK

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 NMT SAFTEY SYRINGE 27GX 1/2" SYRINGE FMF NEW MEDICAL TECHNOLOGY, INC. 20017 (SEE ATTACHED) 08-2005

Patients

Seq Age Sex Outcome Treatment
1 35 YR Required Intervention