Ortho-Clinical Diagnostics: Medical Device Recall in 2013 - (Recall #: Z-1649-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

VITROS 5600 Integrated System (product code 6802413) 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.

Product Classification:

Class II

Date Initiated: May 6, 2013

Date Posted: July 10, 2013

Recall Number: Z-1649-2013

Event ID: 65207

Reason for Recall:

There is evidence that an electrical short within the systems connector has caused an accumulation of heat which has radiated back through the wiring harness causing the wires and connectors to melt.

Status: Terminated

Product Quantity: Total 381 units ( 227 units domestically & 154 units internationally)

Code Information:

Serial numbers: J56000110, J56000118 and J56001095 through J56001507

Distribution Pattern:

Worldwide Distribution - USA Nationwide including the states of AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NY, OH, OK, OR, PA, SC, SD, TN, TX, VA, WA, WI & WV, and countries of: Australia, Brazil, Canada, Chile, China, Colombia, India, Japan, Mexico, PR, Panama, Singapore, Venezuela, England, France, Germany, Italy, Spain

Voluntary or Mandated:

Voluntary: Firm initiated