ADRIA SRL

FDA Regulatory Profile

Summary

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

Recent Recalls

NumberClassProductDate
Z-0144-2022Class IIHerniatome, 17G x 15cm, Lumbar Type with with 20ga-30cm Introducer, Model Number 5091715May 17, 2021
Z-0145-2022Class IIHerniatome, 17G x 15cm, Lumbar Type, Model Number 5091745May 17, 2021
Z-0146-2022Class IIHerniatome, 17G x 9cm, Cervical Type, Model Number 5091749May 17, 2021