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Siemens Healthcare Diagnostics, Inc. recalls N Cuvette Segments for BN ProSpec System-IVD a system for the quantitative determination of proteins in serum, plasma, u
Recalled August 28, 2019 · FDA recall Z-2341-2019 · Siemens Healthcare Diagnostics
Hazard
Iincreased (falsely elevated) Albumin results compared to expected results · FDA Class II
Units
664 units
Sold at
Nationwide
Description
Iincreased (falsely elevated) Albumin results compared to expected results
Product
N Cuvette Segments for BN ProSpec System-IVD a system for the quantitative determination of proteins in serum, plasma, urine and CSF. Siemens Material Number (SMN):10446539
Manufacturer(s)
Siemens Healthcare Diagnostics, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →