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Philips Recalls BrightView Imaging Systems Due to the Detector Unexpectedly Falling
Please be aware, this recall is a correction, not a product removal.
Philips brightview
Philips field service engineer
Drug administration
Adverse event reporting program
Customer care solutions center
Recall database
Single photon emission computed tomography
Computed tomography
Brightview camera systems
Urgent medical device correction
Philips North America LLC Recalls Panorama 1 0T HFO Due to a Risk of Explosion
The FDA has identified this as a Class I recall, the most serious type of recall
Drug administration
Adverse event reporting program
Philips north america
Customer care solutions center
Device correction
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