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N LATEX FLC KAPPA

Siemens Healthcare Diagnostics Products GmbH · Model 10873629 · UDI-DI 00630414167657

DFH
10
510(k) clearances
55
Adverse events
2
Recalls
18
Facilities

Description

Quantitative determination of free light chains (FLC) type kappa in human serum and EDTA-plasma on Siemens analyzers

Recalls

DateFirmReason
2021-05-20The Binding Site Group, Ltd.The high and low level "Quality Controls" demonstrate a positive bias of approximately 10% compared to assigned values.
2020-11-18The Binding Site Group, Ltd.Due to customer complaints of positive bias impacting quality control. The high and low level controls are demonstrating a positive bias compared to assigned values.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.