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Torrent Suite™ Dx SW, V5.6.4

LIFE TECHNOLOGIES HOLDINGS PTE. LTD. · Model A33178 · UDI-DI 10190302005654

PFF Prescription
2
510(k) clearances
8
Adverse events
18
Recalls
13
Facilities

Description

KIT, TS DX SW V5.6.4

Recalls

DateFirmReason
2026-08-14Life Technologies Holdings Pte LtdDNA or RNA sequencing system software has vulnerabilities.
2024-09-17Illumina, Inc.Retrospectively reported correction for an instrument intended for targeted sequencing of DNA libraries from human genomic DNA used with in vitro diagnostic assays has a server wit
2024-05-08Illumina, Inc.(Retrospectively reported) Cybersecurity vulnerability identified in communication protocol between the customer-provided infrastructure (network storage, servers, or computers) an
2024-05-08Illumina, Inc.(Retrospectively reported) Cybersecurity vulnerability identified in communication protocol between the customer-provided infrastructure (network storage, servers, or computers) an
2024-05-08Illumina, Inc.(Retrospectively reported) Cybersecurity vulnerability identified in communication protocol between the customer-provided infrastructure (network storage, servers, or computers) an
2024-05-08Illumina, Inc.(Retrospectively reported) Cybersecurity vulnerability identified in communication protocol between the customer-provided infrastructure (network storage, servers, or computers) an
2024-05-08Illumina, Inc.(Retrospectively reported) Cybersecurity vulnerability identified in communication protocol between the customer-provided infrastructure (network storage, servers, or computers) an
2024-02-07Life Technologies CorporationTorrent Suite Dx Software versions 5.14 and earlier used in connection with Ion PGM DX Systems exploitation of the vulnerability by a threat actor may allow them to alter settings,
2023-04-05Illumina, Inc.Cybersecurity vulnerability concerning the software used for sequencing instruments.
2023-04-05Illumina, Inc.Cybersecurity vulnerability concerning the software used for sequencing instruments.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.