{"id":35633,"date":"2022-06-03T22:09:20","date_gmt":"2022-06-03T22:09:20","guid":{"rendered":"https:\/\/harchi90.com\/illumina-cybersecurity-vulnerability-may-present-risks-for-patient-results-and-customer-networks-letter-to-health-care-providers\/"},"modified":"2022-06-03T22:09:20","modified_gmt":"2022-06-03T22:09:20","slug":"illumina-cybersecurity-vulnerability-may-present-risks-for-patient-results-and-customer-networks-letter-to-health-care-providers","status":"publish","type":"post","link":"https:\/\/harchi90.com\/illumina-cybersecurity-vulnerability-may-present-risks-for-patient-results-and-customer-networks-letter-to-health-care-providers\/","title":{"rendered":"Illumina Cybersecurity Vulnerability May Present Risks for Patient Results and Customer Networks: Letter to Health Care Providers"},"content":{"rendered":"
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June 2, 2022<\/p>\n

The US Food and Drug Administration (FDA) is informing laboratory personnel and health care providers about a cybersecurity vulnerability affecting software in the Illumina NextSeq 550Dx, the MiSeqDx, the NextSeq 500, NextSeq 550, MiSeq, iSeq, and MiniSeq, next generation sequencing instruments . These instruments are medical devices that may be specified either for clinical diagnostic use in sequencing a person’s DNA or testing for various genetic conditions, or for research use only (RUO). Some of these instruments have a dual boot mode that allows a user to operate them in either clinical diagnostic mode or RUO mode. Devices intended for RUO are typically in a development stage and must be labeled \u201cFor Research Use Only. Not for use in diagnostic procedures. ” – though many laboratories may be using them with tests for clinical diagnostic use.<\/p>\n

The cybersecurity vulnerability affects the Local Run Manager (LRM) software. An unauthorized user could exploit the vulnerability by:<\/p>\n