FDA Adverse Event Other Summary report: N

SHARPSSTAR IN-ROOM SHARPS DISPOSAL CONTAINER

MDR report key: 176053 · Received July 7, 1998

Report

Report Number
1419181-1998-00075
Event Type
Other
Date Received
July 7, 1998
Report Date
July 6, 1998
Manufacturer
SAGE PRODUCTS, INC.
Product Code
MMK
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

REPORTER DESCRIBED EVENT AS FOLLOWS: A NURSE PLACED A NEEDLE/SYRINGE INTO THE LID/DOOR OF THE SHARPS CONTAINER. THE NURSE "FLIPPED" INSTEAD OF LIFTING THE LID/DOOR AND REPORTEDLY SOMEHOW REC'D A NEEDLESTICK.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SHARPSSTAR IN-ROOM SHARPS DISPOSAL CONTAINER SHARPS DISPOSAL CONTAINER MMK SAGE PRODUCTS, INC. 8509 UNK

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN