FDA recall Z-2879-2020

Ortho Clinical Diagnostics · Class II · device

Product

VITROS XT7600 Integrated System, Product code 6844461

Reason for recall

When processing MicroSlides, slides that utilize Slot 18 in the CM rotor may be mis-positioned. As a result, certain VITROS MicroSlides may produce erroneous results.

Distribution

Worldwide distribution - US Nationwide distribution and the countries of Australia, Belgium, Brazil, Canada, Chile, China, Colombia, Denmark, France, Germany, India, Italy, Japan, Mexico, Norway, Poland, Portugal, Russia, Singapore, Spain, Sweden, The Netherlands, United Kingdom.

Key facts

Status
Terminated
Initiation date
2020-07-20
Report date
2020-09-02
Termination date
2023-12-18
Voluntary/Mandated
Voluntary: Firm initiated
Location
Rochester, NY, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2879-2020