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 |
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