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DImension Vista® Cystatin C Flex® reagent cartridge

Siemens Healthcare Diagnostics Products GmbH · Model 10445895 · UDI-DI 00842768006104

NDY
1
510(k) clearances
21
Adverse events
4
Recalls
24
Facilities

Description

For the quantitative measurement of cystatin C in human serum and plasma on the Dimension Vista® System

Recalls

DateFirmReason
2024-06-07Randox Laboratories Ltd.Cystatin C Reagent marketed without a 510 (k)
2024-02-14Randox Laboratories Ltd.Cystatin C Calibrator Series CVS 2699, is running with a negative bias compared to other methods
2020-09-02Gentian ASThe firm has identified lots of calibrators that have shown to measure incorrect high values over time compared to the assigned values when released for distribution. This could re
2018-03-05Tosoh Bioscience IncAsfotase Alfa (Strensiq) interferes with certain Tosoh assays which potentially causes falsely increased or falsely decreased immunoassay test results, depending upon the assay.

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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.