Per the following link there appears to be four pages of patient complaints regarding faulty Lyme disease antibody testing and subsequent misdiagnosis. MAUDE - Manufacturer and User Facility Device Experience http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmaude/TextResults.cfm?dls=1&q=lyme&pf=&pn=10&sc= Please take a moment to file a complaint of how these tests affected your Lyme disease diagnosis: https://www.accessdata.fda.gov/scripts/medwatch/index.cfm?action=consumer.reporting1 Please continue to promote this petition. Thank you! Petition: Calling for a Congressional investigation of the CDC, IDSA and ALDF https://www.change.org/petitions/the-u-s-senate-calling-for-a-congressional-investigation-of-the-cdc-idsa-and-aldf