San Giovanni In Persiceto, N/A, Italy
ADRIA SRL recalls
1 recall recorded since 2018, most recently on 17 May 2021. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 17 May 2021
- Terminated
- 6 November 2023
- Reason
- The recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed.
- Distribution
- The products were distributed to the following US states: NJ and NY.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-0145-2022, Z-0146-2022, Z-0144-2022
- Herniatome, 17G x 15cm, Lumbar Type, Model Number 5091745
- Herniatome, 17G x 9cm, Cervical Type, Model Number 5091749
- Herniatome, 17G x 15cm, Lumbar Type with with 20ga-30cm Introducer, Model Number 5091715
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.