Siemens Healthcare Diagnostics, Inc. recalls Analyzer and Atellica IM 1600 Analyzer system for in vitro d
Recalled Product
Analyzer and Atellica IM 1600 Analyzer system for in vitro diagnostic testing of clinical specimens.
Hazard / Issue
When more than one immunoassay analyzer is connected to a single solution system, reporting and conversion factors may not be applied to all analyzers
Issued by
FDA
Affected States: FL
Lot/Code Info: UDI 00630414002026
View official government recall
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