ClearanceBrief
Recall Z-1976-2023 ยท PFF High Throughput Dna Sequence Analyzer

Illumina, Inc.

NextSeq 550Dx Instrument, Catalog # 20005715, contaning Universal Copy Service software

DateJun 16, 2023 (initiated Apr 5, 2023)
StatusCompleted
ReasonCybersecurity vulnerability concerning the software used for sequencing instruments.
Root causeSoftware Manufacturing/Software Deployment
ActionOn April 5, 2023, Illumina issued a "Urgent Medical Device Recall" Notification via XXX. Illumina ask consignees to take the following actions: 1. Download & Install Software Patch: For Each Instrument Connected to the Internet: 2. Change UCS User Configuration(s): Change the UCS User configuration to standard user (with no administrator permissions) by following the instructions available in the customer communication. 3. Complete and return the Verification Form after carrying out all the steps in the instructions provided on your specific instrument(s) identified as affected in Table 1
Quantity1067 units
DistributionWorldwide distribution - US Nationwide and the countries of Algeria, AU Australia, Austria, Belgium, Bulgaria, Canada, Chile, China, Cyprus, Czech Republic, Denmark, Egypt, FR France, GB Georgia, Germany, Guatemala, Hong Kong, Hungary, IT Italy, Japan, Latvia, Lithuania, Luxembourg, Macedonia, Malt
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.