What are the steps for disconnecting a unit implicated in a label error?

The correct answer involves generating an incomplete PDA report and delivering it to Center QA because this step is crucial in documenting the label error while ensuring that the situation is addressed appropriately according to protocols. The report serves as a formal record of the incident, allowing for proper tracking and investigation by quality assurance personnel. This process also helps maintain compliance with regulatory standards, as accurately documenting errors is a key aspect of quality control in plasma collection centers.

By following this step, you ensure that there is a systematic approach to addressing potential safety risks related to errors in labeling. This way, immediate actions can be taken to prevent any complications or adverse effects from the mislabeled unit. Taking this route reflects an emphasis on safety and adherence to established procedures, which is vital in the healthcare and plasma donation fields.