Siemens Healthcare Diagnostics, Inc. recalls Atellica IM Enhanced Estradiol (eE2) (REF) 500T - In vitro d
Recalled Product
Atellica IM Enhanced Estradiol (eE2) (REF) 500T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 11206250 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)00630414293639(10)01380084(17)20220804 (01)00630414293639(10)20299080(17)20220303
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