Account Code:
Type of Incident:
Date of report:
Alleged Incident Date:
Facility Address:
Reporting Persons Name and Title:
Reporting Persons phone# and/or email:
Product Name:
Reorder #:
Expiration Date:
Quantity:
Unit of Measure:
Purchase Order/Invoice #:
Invoice or SO#, If Available:
Brand Name:
Description of Product (as it appears on):
Intended Use (as it appears on label):
Batch/Lot No.:
Serial Number:
Product Returned:
Did you return the product?:
Did any of the following happen?:
Date the problem occurred (mm/dd/yyyy):
Tell us what happened and how it happened*:
Medical or Procedural Intervention?*:
Relevant Tests/Laboratory Data:
Test Date:
Test Name:
Test Unit:
Test Result:
Low Test Range:
High Test Range:
Additional Comments:
Please select the cause of the problem that applies below:
If it's a medical device, select any that apply:
Do you still have the product in case we need to evaluate it?:
Do you have a picture of the product/defect? :