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

Recall Z-2191-2013 — Vision One Laser System Model GA-0025020, Serial No: 10050, 10051, 10053. Intended for use in the treatment of ocular pathology.

U.S. FDA — Device Enforcement · United States · 2013-08-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2191-2013
Date of alert
2013-08-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Lumenis, Inc.
Product category
device
Product type
Devices
Reported risk: Lumenis has initiated a recall on certain models of Vision One System due to a potential for unintended laser exposure to the user.
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.