FDA Enforcement Class II Terminated

VITROS 5600 Chemistry System, Catalog Number 6802413, Unique Device Identifier Number 10758750002740; IVD. Product Usage: For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Chemistry Products Slides, VITROS Chemistry Products MicroTip Reagents and VITROS Immunodiagnostic Products Reagents.

Recall: Z-1074-2016 · Reported March 16, 2016

Enforcement

Recall Number
Z-1074-2016
Event ID
72979
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Ortho-Clinical Diagnostics
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
March 16, 2016
Initiation Date
December 21, 2015
Classification Date
March 8, 2016
Termination Date
May 30, 2018
Address
100 Indigo Creek Dr, N/A, Rochester, NY, 14626-5101, United States

Description

VITROS 5600 Chemistry System, Catalog Number 6802413, Unique Device Identifier Number 10758750002740; IVD. Product Usage: For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Chemistry Products Slides, VITROS Chemistry Products MicroTip Reagents and VITROS Immunodiagnostic Products Reagents.

Reason

Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1 FS, 4600 and 5600 Chemistry Systems when using Calibrator Kit 9, Lot 954. A trend of complaints regarding customers actions following U90-382 or 6LU condition codes was noted (See RES 72289 - VITROS Calibrator Kit 9, lot 954 recall).

Code Info

Software Version 3.2 and below; Serial Numbers J56000024 - 56002339

Distribution

Worldwide Distribution - US Nationwide including Puerto Rico, and the countries of Australia, Brazil, Canada, Chile, China, Colombia, England, France, Germany, India, Italy, Japan, Mexico, Panama, Singapore, Spain, and Venezuela

Quantity

US = 1009; Foreign = 1003