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Siemens Healthcare Diagnostics, Inc recalls Dimension Vista LOCI Progesterone; Catalog Number: K6464; Siemens Material Number: 10461743 Product Usage: For in vi
Recalled March 15, 2017 · FDA recall Z-1419-2017 · Siemens Healthcare Diagnostics
Hazard
DHEA-S causes falsely elevated progesterone results. · FDA Class II
Units
1148
Sold at
US Nationwide distribution including Puerto Rico
Description
DHEA-S causes falsely elevated progesterone results.
Product
Dimension Vista LOCI Progesterone; Catalog Number: K6464; Siemens Material Number: 10461743 Product Usage: For in vitro diagnostic use in the quantitative determination of progesterone in serum and using the ADVIA Centaur¿, ADVIA Centaur XP, ADVIA Centaur XPT and ADVIA Centaur CP systems
Manufacturer(s)
Siemens Healthcare Diagnostics, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →