Fresenius Vial Sa

FDA Regulatory Profile

Fresenius Vial Sa appears in FDA public data with 1 recall, 0 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (Z-0362-2019, Class II) was initiated on December 2, 2017.

Summary

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

Recent Recalls

NumberClassProductDate
Z-0362-2019Class IIVolumat MC Agilia Volumetric Infusion Pump, Model No. Z021135, Software version 1.7. Product Usage -December 2, 2017