A pharmacist receives an urgent notification from a manufacturing company for a recall of a specific medication because it may cause serious adverse health issues or death. What type of drug recall is this?

In this scenario, the correct classification of the drug recall is Class I. Class I recalls are designated for products that pose a significant risk of causing serious adverse health consequences or death. This aligns with the situation described, where the medication in question can potentially lead to serious health issues or even death.

Class I recalls are the most serious type of recall issued by the FDA since they pertain to the highest level of threat to patient safety. When a recall is classified as Class I, it necessitates immediate notification to healthcare providers and patients so they can take appropriate actions to mitigate any risks. This might include stopping the use of the medication, returning it, or disposing of it safely.

In contrast, Class II recalls involve products that may cause temporary or medically reversible adverse effects, while Class III recalls are for products that are not likely to cause any adverse health effects but violate manufacturing regulations. Thus, the nature of the notification received by the pharmacist indicates a significant risk level that justifies the Class I classification.