Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0145-2022 — Herniatome, 17G x 15cm, Lumbar Type, Model Number 5091745

U.S. FDA — Device Enforcement · Italy · 2021-05-17 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0145-2022
Date of alert
2021-05-17
Country / jurisdiction
Italy
Risk level
Class II
Risk type
recall
Brand
ADRIA SRL
Product category
device
Product type
Devices
Reported risk: The recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.