FDA Device recall Z-0145-2022
Herniatome, 17G x 15cm, Lumbar Type, Model Number 5091745
- FDA Device
- Class II
- terminated
- Published 2021-10-27
On 2021-10-27 the FDA classified a Class II recall of Herniatome, 17G x 15cm, Lumbar Type, Model Number 5091745 by Adria Srl, citing the recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0145-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-05-17 |
| Published | 2021-10-27 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Adria Srl |
| Distribution | NJ, NY |
Product
Herniatome, 17G x 15cm, Lumbar Type, Model Number 5091745
Reason
The recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed.
Identifiers
| code_info | Lot Number: ZV0994 AD0314/20 AD0316/20 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0145-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.