NeuMoDx Molecular Inc 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 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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
Brand
NeuMoDx Molecular Inc
Lot Codes / Batch Numbers
GTIN: 10814278020274 Lot Numbers: 117514, 117524, and 117528
Products Sold
GTIN: 10814278020274 Lot Numbers: 117514, 117524, and 117528
NeuMoDx Molecular Inc is recalling NeuMoDx Cartridge-used for extraction, purification, amplification and detection of nucleic acids on due to Top label on some of the NeuMoDx cartridges within these lots may have been incorrectly applied during the manufacturing process, resulting in encroac. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Top label on some of the NeuMoDx cartridges within these lots may have been incorrectly applied during the manufacturing process, resulting in encroachment into the PCR region. The misplaced label may interfere with the module s optics performance, thereby increasing the risk for false positive results
Recommended Action
Per FDA guidance
Qiagen issued customers "Urgent: Medical Device Correction" Letter via email on 5/24/23. Letter states reason for recall, health risk and action to take: If you have remaining stock of cartridges LOT 117514, 117524 or 117528, REF 100100, do not use it. Please contact QIAGEN Technical Service for a free-of-charge replacement. Dispose of the product LOT 117514, 117254, and 117528 in accordance with your national and local safety and environmental regulations. If you have already used NeuMoDx Cartridges from this LOT, please review all results obtained with the laboratory director and assess whether retesting is required. Review this notice with your laboratory/medical director. Important: Forward this information to all individuals and departments within your organization using the above listed cartridges. If you are not the end user, please forward this notice to the product end user. Complete Acknowledgement of Receipt attached to this letter by as soon as possible. If you have any questions or concerns, please contact your local QIAGEN Technical Service Department through any of the following: www.qiagen.com/QIAGEN-Subsidiaries.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026