Class II — Potential Health Hazard

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

Acrobat 3000 (AC3000) Spring Arm as support arm for iLED operating lights Recalled by Trumpf Medical Systems, Inc. Due to Cracks can arise on the welded seam on...

Date: May 29, 2012
Company: Trumpf Medical Systems, Inc.
Status: Terminated
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

Acrobat 3000 (AC3000) Spring Arm as support arm for iLED operating lights, TRUMPF Medizinsysteme GmbH + Co KG 82178 Puchheim. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patients body with a high intensity light.

Quantity: 402 units

Why Was This Recalled?

Cracks can arise on the welded seam on the rear joint.

Where Was This Sold?

This product was distributed to 7 states: CA, NY, OH, OK, PA, TX, WY

Affected (7 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