Siemens Healthcare Diagnostics, Inc. recalls ADVIA Centaur Enhanced Estradiol (eE2) (REF) 500T - In vitro
Recalled Product
ADVIA Centaur Enhanced Estradiol (eE2) (REF) 500T - In vitro diagnostic use in the quantitative detection of estradiol SMN: 10697757 All lots
Hazard / Issue
Falsely Elevated Results Observed with Plasma Specimens, could lead a clinician to misinterpret patient results
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: All lot numbers UDI: (01)00630414591056(10)13852076(17)20220115 (01)00630414591056(10)46894074(17)20211028 (01)00630414591056(10)89042083(17)20220805
View official government recall
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