Brand Name: DASH Rapid PCR Instrument Product Name: DASH Rapid PCR Instrument Model/Catalog Number: SG-0002 Software Version: 6.0.2 Product Description: The DASH Rapid PCR Instrument (DASH Instrument) is an automated, fluorescence-based, reverse-transcription polymerase chain reaction (RT-PCR) instrument that extracts specimens and performs nucleic acid amplified tests (NAAT) in DASH test cartridges for the qualitative detection of infectious diseases. The DASH Instrument is intended for use in conjunction with DASH Rapid PCR System tests to aid in the diagnosis of infectious diseases. Component: No.
FDA Recall Z-2861-2026 · Posted 2026-08-03
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Recalling FirmNuclein LLC
Recall StatusOpen, Classified
Product CodeNSU
Date Initiated2025-06-25
Product Quantity2
Reason for Recall
Due to a software issue which may result in false co-infection (e.g., Positive for Flu A, when SARS-CoV-2 is present).
Firm Action
On 06/25/2025, a "MEDICAL DEVICE RECALL" Letter was emailed to customers informing them that, Nuclein identified an incorrect software file on a small number of DASH instruments that creates a possibility for the affected instruments to make incorrect calls that indicate coinfection in the patient tested.
On 07/16/2026, the firm emailed an updated "URGENT: MEDICAL DEVICE RECALL" Letter.
-Customer were informed regarding updates to the reason for the recall and potential health risks.
-Customer were instructed to:
All affected DASH Instrument identified in Section 6 (below) have already been replaced.
Please complete the Acknowledgement and Receipt Form below and either email the completed form to [email protected] or mail to the address provided at the bottom of the Acknowledgement and Receipt Form.
For Questions - contact Nuclein at Phone: (888) 992-DASH on Monday through Friday, 8:30 AM to 5:30 PM, CST.
Email: [email protected]
Website: https://www.Nuclein.com/contact-us/
Root Cause
Process control
Distribution Pattern
US Nationwide distribution in the state of Texas.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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