Ortho-Clinical Diagnostics: Medical Device Recall in 2016 - (Recall #: Z-0640-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

VITROS 3600 Chemistry System, Catalog Number 6802783, Unique Device Identifier Number 10758750009930, Software Product Code 6802866, Software Version 3.2 and below; 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 Immunodiagnostic Products Reagents.

Product Classification:

Class II

Date Initiated: November 3, 2015

Date Posted: January 20, 2016

Recall Number: Z-0640-2016

Event ID: 72597

Reason for Recall:

Software anomaly may allow VITROS Systems to sample and process assays while the fluids and reagent temperatures are not in the required temperature range for optimal processing. When this intermittent issue occurs, the VITROS Systems continue to operate and process results without notification to the User, possibly producing erroneous results.

Status: Terminated

Product Quantity: Domestic: 200, Foreign: 554

Code Information:

Software Version 3.2 and below; Serial Numbers J36000012 - 36000879

Distribution Pattern:

Worldwide Distribution - US Nationwide and the countries of Puerto Rico, and foreign distribution to: Argentina, Australia, Brazil, Canada, Chile, China, Colombia, England, France, Germany, India, Israel, Italy, Japan, Kenya, Mexico, Panama, Philippines, Poland, Romania, Russia, Singapore, Spain, Taiwan, Turkey, and Venezuela.

Voluntary or Mandated:

Voluntary: Firm initiated