Question

Your pharmacy receives a notice that Flomax capsules were recently part of a Class II recall. How is this recall best described?

a) Minor risk of adverse effects

b) Serious risk of adverse effects

c) No risk of adverse effects

d) Voluntary removal by the manufacturer

Answer 1

A Class II recall is best described as a serious risk of adverse effects.

Step-by-step explanation:

The best description of a Class II recall is b) Serious risk of adverse effects.

In the case of Flomax capsules being part of a Class II recall, it means that there is a significant risk of adverse effects associated with the use of these capsules. This could be due to a manufacturing defect, labeling issue, or potential contamination.

Examples of serious adverse effects may include severe allergic reactions, life-threatening events, or long-term health consequences.