ADRIA SRL: Medical Device Recall in 2021 - (Recall #: Z-0144-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Herniatome, 17G x 15cm, Lumbar Type with with 20ga-30cm Introducer, Model Number 5091715

Product Classification:

Class II

Date Initiated: May 17, 2021

Date Posted: October 27, 2021

Recall Number: Z-0144-2022

Event ID: 88543

Reason for Recall:

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

Status: Terminated

Product Quantity: N/A

Code Information:

Lot Number: AD0316/20

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated