medical Class II Updated 2022-05-11

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

Looking for safe alternatives?

Browse certified-safe products in this category on Amazon →