ADRIA SRL Recall 88543
Description: Herniatome, 17G x 9cm, Cervical Type, Model Number 5091749
ADRIA SRL Recall 88543 Information
| Status | Ongoing |
| Mandated? | Voluntary: Firm initiated |
| Recall Number | Z-0146-2022 |
| Event ID | 88543 |
| Event Description | Herniatome, 17G x 9cm, Cervical Type, Model Number 5091749 |
| Product Type | Devices |
| Distribution | The products were distributed to the following US states: NJ and NY. |
| Recall Reason | The recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed. |
| Device Classification | 20211027 |
| Device Code Info | Lot Number: AD0063/20 AD0313/20 AD0302/20 |
| Center Classification Date | 20211019 |
| Recall Initiation Date | 20210517 |
| Recalling Firm | ADRIA SRL |
| Initial Notification | Letter |
| Similar To |