Agilent Technologies Denmark ApS

FDA Regulatory Profile

Agilent Technologies Denmark ApS appears in FDA public data with 3 recalls, 0 510(k) clearances, 2 FDA inspections, and 1 compliance action on record. Its most recent recall (Z-2563-2025, Class II) was initiated on August 11, 2025.

Summary

Total Recalls
3
510(k) Clearances
0
Inspections
2
Compliance Actions
1

Recent Recalls

NumberClassProductDate
Z-2563-2025Class IIBrand Name: FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use (Dako Omnis) Model/CatAugust 11, 2025
Z-2565-2025Class IIBrand Name: FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use (Dako Omnis) Model/CatAugust 11, 2025
Z-2564-2025Class IIBrand Name: FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use (Dako Omnis) Model/CatAugust 11, 2025