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

Recall Z-2409-2023 — Legion FMS Pak

U.S. FDA — Device Enforcement · United States · 2023-06-28 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2409-2023
Date of alert
2023-06-28
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Alcon Research, LTD.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
8065753164
Reported risk: Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening with included plastic wrench.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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.