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Siemens Healthcare Diagnostics, Inc recalls ADVIA Centaur Progesterone; Catalog Number: 10310305 10315522 10333111 Product Usage: The PROG method is an in vitro
Recalled March 15, 2017 · FDA recall Z-1418-2017 · Siemens Healthcare Diagnostics
Hazard
DHEA-S causes falsely elevated progesterone results. · FDA Class II
Units
76,107
Sold at
US Nationwide distribution including Puerto Rico
Description
DHEA-S causes falsely elevated progesterone results.
Product
ADVIA Centaur Progesterone; Catalog Number: 10310305 10315522 10333111 Product Usage: The PROG method is an in vitro diagnostic test for the quantitative measurement of progesterone in human serum and plasma on the Dimension Vista¿System. Progesterone measurements are used in the diagnosis and treatment of disorders of the ovaries or placenta.
Manufacturer(s)
Siemens Healthcare Diagnostics, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →