class i recall造句

In April 2013, the Food and Drug Administration issued a Class I Recall for the Animas 2020.
Class I recalls are the most severe and indicate that exposure and / or consumption of the drug will lead to adverse health effects or death.
On April 25, 2008, the FDA issued a press release alerting the public to a Class I recall of Digitek, a brand of digoxin produced by Mylan.
For example, from 2008 to 2011, in US, there were 119 FDA recalls of medical devices classified as class I . According to U . S . Food and Drug Administration ( FDA ), Class I recall is associated to " a situation in which there is a reasonable probability that the use of, or exposure to, a product will cause serious adverse health consequences or death"
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