FDA recall Z-1222-2022

Dynex Technologies, Inc. · Class II · device

Product

DYNEX Agility, Agility Analyzer, Model No. 67000

Reason for recall

Control samples aspirated from wrong SmartKit on the Agility. Agility software was updated to v1.4.7 to resolve the issue. This leads to a risk that a control from another assay's SmartKit will be used instead of the correct control, which may lead to delayed patient results.

Distribution

Worldwide distribution - US Nationwide distribution in the states of AL, CA, DC, FL, GA, IL, IN, MA, MD, MI, NE, NJ, NY, OH, PA, PR, TN, TX, UT, VA, WI, WV and the countries of Belgium, Brazil, China, Czech Republic, France, Germany, Mexico, Qatar, Romania, Russia, South Korea, Switzerland, Taiwan, and UK.

Key facts

Status
Ongoing
Initiation date
2020-07-05
Report date
2022-06-08
Voluntary/Mandated
Voluntary: Firm initiated
Location
Chantilly, VA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1222-2022