FDA Adverse Event Injury Summary report: N

BACT/ALERT MP BOTTLE

MDR report key: 495651 · Received August 14, 2003

Report

Report Number
1039284-2003-00003
Event Type
Injury
Date Received
August 14, 2003
Date of Event
March 18, 2003
Report Date
August 14, 2003
Manufacturer
BIOMERIEUX, INC.
Product Code
JTA
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

HOSPTIAL EMPLOYEE WAS TRYING TO REMOVE THE METAL CRIMP FROM A BACT/ALERT MP BOTTLE. EMPLOYEE WAS USING FORCEPS AND WAS CUT THROUGH THE GLOVES. BASIC FIRST AID WAS APPLIED. ANTISEPTIC SPRAY AND A BANDAID WERE APPLIED TO THE CUT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BACT/ALERT MP BOTTLE MICROBIAL GROWTH MONITOR JTA BIOMERIEUX, INC. * 212201

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Other