Siemens Healthcare Diagnostics, Inc. recalls Atellica IM Enhanced Estradiol (eE2) 100T - In vitro diagnos
Recalled Product
Atellica IM Enhanced Estradiol (eE2) 100T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10995561 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)00630414598857(10)53376082(17)20220521 (01)00630414598857(10)53377082(17)20220521 (01)00630414598857(10)70533084(17)20220804
View official government recall
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