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NeuMoDx Molecular Inc: Medical Device Recalls in 2023

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by NeuMoDx Molecular Inc in 2023. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.
See this for other years:
2021
2022
2023
  • 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
  • NeuMoDx Cartridge-used for extraction, purification, amplification and detection of nucleic acids on the NeuMoDx 288 and NeuMoDx 96 Molecular Systems (NeuMoDx System(s) Ref: 100100
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