RecallRadar

FDA Device recall Z-1074-2016

VITROS 5600 Chemistry System, Catalog Number 6802413, Unique Device Identifier Number 10758750002740

On 2016-03-16 the FDA classified a Class II recall of VITROS 5600 Chemistry System, Catalog Number 6802413, Unique Device Identifier Number 10758750002740 by Ortho Clinical Diagnostics, citing 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 regardin….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1074-2016
ClassificationClass II
Statusterminated
Initiated2015-12-21
Published2016-03-16
Last updated2026-09-13 11:54 UTC
CompanyOrtho Clinical Diagnostics
DistributionUS

Product

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).

Identifiers

code_infoSoftware Version 3.2 and below; Serial Numbers J56000024 - 56002339

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1074-2016%22

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