ADRIA SRL Herniatome, 17G x 15cm, Lumbar Type with with 20ga-30cm Introducer, Model Number recall — FDA Z-0144-2022
The recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed.
Overview of recall records associated with ADRIA SRL, including dates, categories and classifications where available.
Classification mix: Class II: 1.
The recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed.
This page summarizes recall records in which the official source identifies ADRIA SRL as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.