Which of the following must be included when completing a phlebotomy related exposure incident report?

The inclusion of the type of device used to collect the specimen in a phlebotomy-related exposure incident report is crucial for several reasons. First, it allows for an understanding of the circumstances surrounding the exposure. Different devices have varying safety features and risks associated with them, so identifying the specific device helps in assessing whether appropriate procedures and precautions were followed.

Additionally, documenting the device can aid in evaluating whether the exposure incident could be prevented by using different equipment or implementing better safety measures. Understanding the specifics of the equipment used is essential for ongoing safety training and policy adjustments in the laboratory or healthcare setting.

In contrast, while the date of the procedure and the name of the phlebotomist may also be relevant for context and accountability, they do not provide the same level of detail about the low-level risks associated with specific devices. Notably, a patient's medical history is typically unrelated to the specifics of the exposure incident and is therefore not pertinent to the report's focus on the incident itself.