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Facilities can use this sample tool to investigate mislabeling events by providing an overview, gathering investigative notes, categorizing errors, and identifying contributing factors to reveal system-related problems.
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How to fill out specimen labeling event investigation

01
Gather all necessary information about the specimen, including patient details and sample type.
02
Clearly label each specimen with unique identifiers, such as barcode or ID number.
03
Document the collection date and time, as well as the person collecting the specimen.
04
Ensure proper handling and storage conditions are noted prior to shipping or analysis.
05
Record any relevant observations or incidents that occurred during the specimen collection process.
06
Review the completed labeling and investigation forms for accuracy before submission.

Who needs specimen labeling event investigation?

01
Laboratory personnel handling specimens.
02
Healthcare providers involved in patient treatment.
03
Quality assurance teams ensuring compliance with labeling standards.
04
Regulatory agencies overseeing laboratory practices.
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Specimen labeling event investigation is a process to investigate discrepancies or issues related to the labeling of biological specimens, ensuring that they are accurately identified and tracked throughout the testing process.
Individuals or organizations involved in the handling, processing, and testing of biological specimens, such as laboratories and healthcare providers, are required to file specimen labeling event investigations when discrepancies occur.
To fill out a specimen labeling event investigation, one should provide detailed information about the specimen in question, including the type of specimen, the nature of the labeling issue, the individuals involved, the timeline of events, and any corrective actions taken.
The purpose of a specimen labeling event investigation is to ensure the integrity and accuracy of specimen identification, reduce the risk of errors in testing and reporting, and maintain patient safety.
The information that must be reported includes the specimen type, details of the labeling discrepancy, the individuals involved, timestamps of the event, potential impacts on test results, and steps taken to resolve the issue.
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