Class II — ADRIA SRL
| Recalling firm | Adria Srl. |
|---|---|
| Registered facility | ADRIA SRL. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed. |
| Product | Herniatome, 17G x 9cm, Cervical Type, Model Number 5091749 |
| Quantity | N/A |
| Distribution | The products were distributed to the following US states: NJ and NY. |
| Initiated | 2021-05-17 |
| Classified | 2021-10-19 |
| Terminated | 2023-11-06 |
| Recall number | Z-0146-2022 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — ADRIA SRL (Z-0146-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/88543/
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