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Recall Observatory FDA recall evidence

Device product

VITROS XT 7600 Integrated System, Product Code 6844461, UDI 1075870031658 Product Usage: The VITROS XT 7600 Integrated System is intended for use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Chemistry Products MicroSlides, VITROS Chemistry Products MicroTip Reagents, and VITROS Immunodiagnostic Products Reagents

Z-1222-2019

March 11, 2019

Class II

Product summary

Firm
Ortho-Clinical Diagnostics
Event
Event 82366
Status
Terminated
Classification
Class II
Quantity
80
Official record key
device-enforcement:Z-1222-2019

Official wording

Reason: One of the software algorithms used to detect sample dispense errors was inadvertently disabled. Because of this, sample dispense errors may lead to incorrect results being reported without an error code to alert the user.

Code information: Systems Running Software Version 3.4 & 3.4.1

Distribution pattern: Worldwide Distribution - US Nationwide in the states of: AZ, CA, FL, IL, OH, TX, and VA. The products were distributed to the following foreign countries: Australia, Belgium, Canada, Chile, Columbia, France, India, Italy, Japan, Portugal, Singapore, Spain, United Kingdom

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software algorithms used to detect sample dispense errors was inadvertently disabled. Because of this, sample dispense errors may