The FDA issues a warning letter to Philips over its late notification for the recall of a component of its InnerCool RTx temperature control device. The FDA dinged Philips (NYSE:PHG) for tardiness in its notification of the recall of a component for its InnerCool RTx body temperature control device in a warning letter sent last month. Philips issued a recall in January 2012 of the main control board for the InnerCool device, which is used to raise or lower the body's core temperature, according to the warning letter.
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