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.
Agilent Technologies
5 recalls • • Categories: Other Medical Devices, Infusion Pumps, Diagnostic Equipment
Class I - Dangerous
There is the potential for the front plexiglass door of the automated slide processing system to break causing potential injury.
Class I - Dangerous
Label provided for substrate vail contained incorrect expiration date.
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.
The product was marketed without 510(k) clearance.