BD KIESTRA LAB AUTOMATION

FDA Regulatory Profile

BD KIESTRA LAB AUTOMATION appears in FDA public data with 1 recall, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1658-2026, Class II) was initiated on February 6, 2026.

Summary

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

Recent Recalls

NumberClassProductDate
Z-1658-2026Class IIBD Kiestra" ReadA; Catalog No.: 446948.February 6, 2026