ClearanceBrief
Recall Z-0042-2025 ยท OCC Respiratory Virus Panel Nucleic Acid Assay System

Luminex Molecular Diagnostics Inc

NxTAG Respiratory Pathogen Panel, REF: I051C0447

DateOct 9, 2024 (initiated Sep 5, 2024)
StatusOpen, Classified
ReasonRespiratory pathogen panel may report an elevated rate (7.6% predicted probability of occurrence) of non-specific hMPV target (human Metapneumovirus) results, risk identified predominantly in clinical samples that present positivity for another target, leading to an erroneous co-infection result, can potentially result in hMPV false positives.
Root causeDevice Design
ActionOn 9/5/24, recall notices were sent to customers and distributors were were asked to do the following: 1. Two options are available to overcome the sporadic potential risk of the hMPV false positive result: A. Continue to use the product as per its instruction for use: in case of a positive result for hMPV, consider performing confirmatory testing with another method before reporting the hMPV result, if medically indicated. B. Exclude the hMPV from the reporting by removing this target from the assay analysis, as explained in the package insert under the chapter "Define Test Panels in SYNCT So
Quantity3375
DistributionU Nationwide distribution in the states of OH, CA, NC, WI, TN, TX, MI, NY, MO, FL, MA, NJ, PA, VA, AZ, IL, OK, CO, MN.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K152386NxTAG Respiratory Pathogen Panel, NxTAG Respiratory Pathogen Panel Files, SYNCT Software
Luminex Molecular Diagnostics, Inc., Dec 17, 2015
K193167NxTAG Respiratory Pathogen Panel, NxTAG Respiratory Pathogen Panel Files, SYNCT Software
Luminex Molecular Diagnostics, Inc., Dec 11, 2019