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Siemens Healthcare Diagnostics, Inc recalls IMMULITE/ IMMULITE 1000 Progesterone; Catalog Number: LKPW1; Siemens Material Number: 10381128 Product Usage: For in
Recalled March 15, 2017 · FDA recall Z-1420-2017 · Siemens Healthcare Diagnostics
Hazard
DHEA-S causes falsely elevated progesterone results. · FDA Class II
Units
9076
Sold at
US Nationwide distribution including Puerto Rico
Description
DHEA-S causes falsely elevated progesterone results.
Product
IMMULITE/ IMMULITE 1000 Progesterone; Catalog Number: LKPW1; Siemens Material Number: 10381128 Product Usage: For in vitro diagnostic use with the IMMULITE¿2000 Systems Analyzers- for the quantitative measurement of progesterone in serum, as an aid 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 →