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Parker Quality & Compliance

PQC Reg Watch

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Device recall

Illumina DRAGEN Server for NextSeq 550Dx REF: 20086130,

FDA recall source

Recall number
Z-0323-2027
Event id
99957
Status
Open, Classified
FDA classification
Class II
Recalling firm
Illumina, Inc.
Posted
Oct 30, 2026
Initiated
May 8, 2024
Product code
PFF
Device type
High Throughput Dna Sequence Analyzer
Reason
(Retrospectively reported) Cybersecurity vulnerability identified in communication protocol between the customer-provided infrastructure (network storage, servers, or computers) and in vitro diagnostic devices which may result in compromised data transmission.
Root cause
Labeling design
Quantity
32 units
Code info
All Lots/UDI: N/A
Distribution
Worldwide - US Nationwide distribution including in the states and territory of AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV and the countries of AE, AR, AT, AU, BE, BG, CA, CH, CL, CN, CY, CZ, DE, DK, DZ, EG, ES, FI, FR, GB, Ghana, GR, GT, HK, HU, IE, IL, IS, IT, JP, KR, KW, LT, LU, LV, MA, MT, NG, NL, NO, NZ, PE, PH, PL, PT, QA, RO, RU, SA, SE, SG, SI, TH, TR, UA, VN, ZA.
Location
San Diego, CA