Skip to content
Recall Observatory FDA recall evidence

Device product

Herniatome, 17G x 15cm, Lumbar Type, Model Number 5091745

Z-0145-2022

May 17, 2021

Class II

Product summary

Firm
ADRIA SRL
Event
Event 88543
Status
Terminated
Classification
Class II
Quantity
N/A
Official record key
device-enforcement:Z-0145-2022

Official wording

Reason: The recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed.

Code information: Lot Number: ZV0994 AD0314/20 AD0316/20

Distribution pattern: The products were distributed to the following US states: NJ and NY.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed.