Agilent Technologies, Inc
5301 Stevens Creek Blvd, Santa Clara, CA, US
Registered product codes
40 product codes
Recent MDR events
1,087 on file
- FLEX MONOCLONAL RABBIT ANTI-HUMAN ESTROGEN RECEPTOR CLONE EP1May 22, 2026Injury0002916205-2026-00001
- FLEX MONOCLONAL MOUSE ANTI-HUMAN PROGESTERONE RECEPTOR CLONE PGR 636 READY-TO-USMay 9, 2025Malfunction3003423869-2025-00029
- GENETISURE DX LABELING KIT, -20C PARTMar 6, 2025Malfunction0002916205-2025-00002
- GENETISURE DX LABELING KIT, -20C PARTFeb 27, 2025Malfunction0002916205-2025-00001
- 405 LS WASHERDec 21, 2023Malfunction0002916205-2023-00003
- 405 LS WASHERDec 20, 2023Malfunction0002916205-2023-00002
- FLX MONO RB A HU PMS2, CL EP51, RTU,LINKAug 22, 2023Malfunction3003423869-2023-00092
- BIOTEK 405 TS WASHERJul 13, 2023Malfunction3003423869-2023-00085
- AGILENT 7000 C GC/MS TRIPLE QUADJun 13, 2023InjuryMW5118386
- PT LINKApr 4, 2023Malfunction3003423869-2023-00044
Recalls
5 on file
- Open, ClassifiedApr 8, 2025
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.
View FDA record ↗ - Open, ClassifiedApr 11, 2023
Distributed sample collection kit with an unapproved instruction for use.
View FDA record ↗ - Open, ClassifiedUnknown
Label provided for substrate vail contained incorrect expiration date.
View FDA record ↗ - TerminatedUnknown
The product was marketed without 510(k) clearance.
View FDA record ↗ - TerminatedUnknown
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.
View FDA record ↗
Compliance history
Matched by FEI 2916205.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.