Trumpf Medical Systems, Inc.: Medical Device Recalls in 2012

According to to data from the FDA, there were 2 medical device recalls made by Trumpf Medical Systems, Inc. in 2012. See the details of the recalls below.

You can see similar recalls for other firms.

• 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.
• Helion and Xenion surgical lights, 501/01 series KLM lights. The surgical lights are intended to locally illuminate an operating or examination area of the patients body with a high intensity light.