Injection drug products continued to be recalled for various
issues. In recent weeks, two injection drug products were recalled,
one for potential sterility issues and a second because consumers
observed particulates floating in some of the vials. Additionally,
a medical device manufacturer that had recalled a peripheral
infusion system in December 2014, due to a device error that arose
from incorrect labeling, issued a second notice stating that the
recall has now been classified by FDA as Class I.
View a complete listing of FDA Recalls.
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