What is the purpose of notifying patients during a Class 1 recall?

The primary purpose of notifying patients during a Class 1 recall is to warn them of potential serious health risks associated with the recalled product. Class 1 recalls are issued when there is a reasonable probability that the use of, or exposure to, a product will cause serious adverse health consequences or death. In essence, the notification serves to protect patient health by ensuring they are aware of the risks involved with the medication, allowing them to take appropriate actions, such as discontinuing use or contacting their healthcare provider for alternatives.

This type of recall is a critical component of public health and safety, emphasizing the importance of communication between healthcare providers, pharmacists, and patients in managing any potential risks resulting from medication use.