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US FDA classifies Philips' recall of imaging machines as most serious

Philips' recall of BrightView Imaging Systems, used for single photon emission computed tomography (SPECT) scan, is to correct the faulty component and not a product removal, the health regulator said. A falling detector may cause a person to experience neck injury, contusion and traumatic brain injury, among others. There has been one incident related to use of the device, but no reports of injuries or deaths, the FDA said.
United States Shounak Dasgupta Shinjini Ganguli Leroy Leo Brightview Imaging Systems Brightview Imaging Systems
Source: yahoo.com

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