ADRIA SRL

FDA Regulatory Profile

ADRIA SRL appears in FDA public data with 3 recalls, 0 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (Z-0144-2022, Class II) was initiated on May 17, 2021.

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-0146-2022Class IIHerniatome, 17G x 9cm, Cervical Type, Model Number 5091749May 17, 2021
Z-0145-2022Class IIHerniatome, 17G x 15cm, Lumbar Type, Model Number 5091745May 17, 2021