FDA recall Z-1587-2018

Siemens Healthcare Diagnostics, Inc. · Class II · device

Product

Atellica Solution and Atellica Sample Handler Prime for in vitro diagnostic testing of clinical specimens.

Reason for recall

When more than one immunoassay analyzer is connected to a single solution system, reporting and conversion factors may not be applied to all analyzers

Distribution

FL and France Spain Sweden United Kingdom Germany

Key facts

Status
Terminated
Initiation date
2018-02-26
Report date
2018-05-09
Termination date
2020-05-12
Voluntary/Mandated
Voluntary: Firm initiated
Location
Tarrytown, NY, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1587-2018