FDA Device recall Z-0144-2022
Herniatome, 17G x 15cm, Lumbar Type with with 20ga-30cm Introducer, Model Number 5091715
- 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 with with 20ga-30cm Introducer, Model Number 5091715 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-0144-2022 |
| 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 with with 20ga-30cm Introducer, Model Number 5091715
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: 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-0144-2022%22
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