A Class I recall indicates what level of health risk?

A Class I recall signifies a situation where there is a reasonable probability that the use of or exposure to a product will cause serious adverse health consequences or death. This classification is used when there is a significant potential for health risks associated with the recalled product, necessitating immediate actions to remove the product from distribution and inform consumers.

Understanding the implications of a Class I recall is crucial for health professionals and consumers alike, as it highlights the seriousness of the risks involved and the importance of swift action to mitigate potential harm. In contrast, other classifications such as Class II and Class III indicate lower levels of risk, where either the health consequences are less likely or there is minimal potential for adverse effects.