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

Recall Z-0484-2014 — Helion S Exam Light or H300 The device is intended to locally illuminate an examination area of the patient's body with high intensity light in a clinic or doctor's practice.

U.S. FDA — Device Enforcement · United States · 2013-02-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0484-2014
Date of alert
2013-02-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Trumpf Medical Systems, Inc.
Product category
device
Product type
Devices
Reported risk: Possible fatigue failure of the plastic joint may occur after an average use of seven years.
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.