FDA recall Z-0435-2022

bioMerieux, Inc. · Class II · device

Product

VIDAS Estradiol II, REF 30431-01

Reason for recall

bioMerieux has been receiving an increasing number of complaints linked to a VIDAS substrate error. It prevents the test from being run, therefore leads to potential delayed results as the user must run another test.

Distribution

US Nationwide distribution.

Key facts

Status
Ongoing
Initiation date
2021-09-22
Report date
2022-01-05
Voluntary/Mandated
Voluntary: Firm initiated
Location
Durham, NC, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0435-2022