Philips Recalled 553 BrightView Imaging Systems in US, FDA Says

Philips has recalled BrightView imaging systems manufactured between Sept. 2007 and June 2013 due to the detector unexpected falling, the US drug regulator said on its website on Feb. 15.

• Philips recalled their BrightView, BrightView X, and BrightView XCT as a falling detector may cause a person to experience neck injury, contusion, traumatic brain injury/concussion, death, crush injury, fracture, laceration, muscle or ligament sprain/strain, as well as an interruption to the system operation
  • There is one reported incident from use of this device; no reports of injuries or deaths
• Philips will contact customers to visit a customer’s site and correct ...