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

Recalled October 27, 2021 · FDA recall Z-0144-2022 · ADRIA SRL

Hazard

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

Units

N/A

Sold at

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

Description

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

Product

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

Manufacturer(s)

ADRIA SRL

Made in

Italy

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →