FDA Adverse Event Injury Summary report: N

LIQUICHEK BLOOD GAS CONTROL CO-OXIMETER

MDR report key: 503034 · Received December 23, 2003

Report

Report Number
2016706-2003-00004
Event Type
Injury
Date Received
December 23, 2003
Date of Event
October 8, 2003
Report Date
December 9, 2003
Manufacturer
BIO-RAD LABORATORIES
Product Code
JJT
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

A LABORATORY EMPLOYEE CUT THEIR FINGER ON AN AMPULE OF QUALITY CONTROL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LIQUICHEK BLOOD GAS CONTROL CO-OXIMETER QUALITY CONTROL MATERIAL JJT BIO-RAD LABORATORIES NA 29080

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Other