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Trumpf Medical Systems, Inc. recalls Acrobat 3000 (AC3000) Spring Arm as support arm for iLED operating lights, TRUMPF Medizinsysteme GmbH + Co KG 82178 Puch
Recalled September 12, 2012 · FDA recall Z-2311-2012 · Trumpf Medical Systems
Hazard
Cracks can arise on the welded seam on the rear joint. · FDA Class II
Units
402 units
Sold at
Worldwide Distribution - USA including CA, OH, OK, NY, PA, TX, WY and the country of Canada
Description
Cracks can arise on the welded seam on the rear joint.
Product
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.
Manufacturer(s)
Trumpf Medical Systems, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →