FDA Identifies Respiratory Devices Recall as Most Serious
The FDA on Monday classified the recall of Philips' respiratory machines as its most serious type, as their use could cause serious injuries or death.
Reuters Health Information
source https://www.medscape.com/s/viewarticle/995463?src=rss
Reuters Health Information
source https://www.medscape.com/s/viewarticle/995463?src=rss
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