FDA Adverse Event Other Summary report: N

LIQUICHEK IMMUNOASSAY PLUS CONTROL

MDR report key: 316825 · Received February 15, 2001

Report

Report Number
2016706-2001-00004
Event Type
Other
Date Received
February 15, 2001
Report Date
February 14, 2001
Manufacturer
BIO-RAD LABORATORIES
Product Code
JJT
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

THE RPTR CALLED TECHNICAL SVCS TO SAY THAT THEY HAD BEEN EXPOSED TO LEVEL 2 CONTROL. AS THEY WERE PLACING THE CAP BACK ON THE CONTROL VIAL, CONTROL MATERIAL ENTERED THEIR EYE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
6070 LIQUICHEK IMMUNOASSAY PLUS CONTROL MULTI-ANALYTE CONTROL (ASSAYED/UNASSAYED) JJT BIO-RAD LABORATORIES NA 40542

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Other