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

Recall Z-0563-2016 — Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted Surgical Light System iLED3/iLED5

U.S. FDA — Device Enforcement · United States · 2015-11-02 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0563-2016
Date of alert
2015-11-02
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Trumpf Medical Systems, Inc.
Product category
device
Product type
Devices
Reported risk: The firm has received 15 complaints over ten years related to the connection of the spring arm to the top horizontal arm of the lighting system that while positioning the light head enabled the spring arm and light head to fall.
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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