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Siemens Healthcare Diagnostics, Inc. recalls Atellica Solution and Atellica Sample Handler Prime for in vitro diagnostic testing of clinical specimens.
Recalled May 9, 2018 · FDA recall Z-1587-2018 · Siemens Healthcare Diagnostics
Hazard
When more than one immunoassay analyzer is connected to a single solution system, reporting and conversion factors may not be applied to all analyzers · FDA Class II
Units
N/A
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Description
When more than one immunoassay analyzer is connected to a single solution system, reporting and conversion factors may not be applied to all analyzers
Product
Atellica Solution and Atellica Sample Handler Prime for in vitro diagnostic testing of clinical specimens.
Manufacturer(s)
Siemens Healthcare Diagnostics, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →