Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted Recalled by Trumpf Medical Systems, Inc. Due to The firm has received 15 complaints over ten...

Date: November 2, 2015
Company: Trumpf Medical Systems, Inc.
Status: Completed
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Trumpf Medical Systems, Inc. directly.

Affected Products

Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted Surgical Light System iLED3/iLED5

Quantity: 20,713

Why Was This Recalled?

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.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Trumpf Medical Systems, Inc.

Trumpf Medical Systems, Inc. has 30 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report