Product Description
NxTAG Respiratory Pathogen Panel +SARS-CoV-2, REF: I056C0468
Reason for Recall
Respiratory 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.
Action Details
On 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 Software". See Document No. and Revision/Page reference: MLD-051-KPI-001 Rev H/Page 17, MLD-056-KPI-001 Rev. E/Page 18.
2. Notify others within your network that may have remaining inventory of those kits.
3. If you are a distributor, provide a copy of this letter to customers or organizations who received impacted lots.
4. Complete and return the response form via email to support@luminexcorp.com
5. For complaints, questions, or concerns, please contact Technical Support using the contact information:
1-877-785-2323 (U.S. and Canada).
+1-512-381-4397 (Outside U.S. and Canada).
1-512-219-5114 (Fax).
support@luminexcorp.com
www.diasorin.com
Distribution Pattern
U 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.
Code Information / Serial Numbers
Lot/Expiration:
IK056C-0033/ 9/30/2024,
IK056C-0034/ 10/31/2024,
IK056C-0035/ 10/31/2024,
IK056C-0036/ 12/31/2024,
IK056C-0037/ 12/31/2024,
IK056C-0038/ 12/31/2024,
IK056C-0039/ 1/31/2025
Public Record Disclaimer
This page represents an index of public-record FDA device recalls. It does not imply current safety or compliance status of the product. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Refer to official government sources for primary safety alerts.