Product Safety Recalls

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ADRIA SRL Recall 88543

Description: Herniatome, 17G x 9cm, Cervical Type, Model Number 5091749

ADRIA SRL Recall 88543 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-0146-2022
Event ID88543
Event DescriptionHerniatome, 17G x 9cm, Cervical Type, Model Number 5091749
Product TypeDevices
DistributionThe products were distributed to the following US states: NJ and NY.
Recall ReasonThe recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed.
Device Classification20211027
Device Code InfoLot Number: AD0063/20 AD0313/20 AD0302/20
Center Classification Date20211019
Recall Initiation Date20210517
Recalling FirmADRIA SRL
Initial Notification Letter
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