Agilent Technologies

5 recalls Categories: Other Medical Devices, Infusion Pumps, Diagnostic Equipment

DNA Labeling Kit for use in sample labeling to be hybridized to oligonucleotide microarrays has a component, Human Reference DNA Female aliquot, affected by a mosaic aberration that may result in Chromosome 12 baseline shift, which may lead to false positive/negative results, resulting in diagnosis delay, and may lead to delayed treatment of a treatable genetic disorder.

Mar 20, 2025 Other Medical Devices View Details →

When utilizing specific software versions of an LC/MS device, and Batch at a Glance in Compound Table view, a defect occurs when a new sample(s) is inserted. This defect creates a mismatch between the sample name and the column header whereby the sample header will be offset by one sample. The recalling firm requests that you discontinue using this workflow to generate reports because the Quant batch table will not display fully analyzed results or save any changes made.

Aug 15, 2018 Diagnostic Equipment Nationwide View Details →

The product was marketed without 510(k) clearance.

Jun 17, 2015 Other Medical Devices View Details →