FDA recall Z-2093-2023

NeuMoDx Molecular Inc · Class III · device

Product

NeuMoDx SARS-CoV-2 Assay -IVD intended for the qualitative detection of SARS-CoV-2 RNA from nasal, nasopharyngeal and oropharyngeal swabs in transport medium and bronchoalveolar lavage (BAL) specimens from individuals suspected of COVID-19 by their healthcare provider (HCP). REF Number: 300800

Reason for recall

Potential for lot number discrepancies between the test strip packaging and the barcode label applied to the test strip that is read by the instrument for LOT 123909 of NeuMoDx SARS-CoV-2 Test Strips (REF 300800). The instrument registers the non-human readable text as lot number 123910 from the barcode label.

Distribution

US Nationwide distribution in the states of FL, MI, NM, NY, TN, TX.

Key facts

Status
Ongoing
Initiation date
2023-05-15
Report date
2023-07-12
Voluntary/Mandated
Voluntary: Firm initiated
Location
Ann Arbor, MI, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2093-2023