Torrent Suite DX SW, Installer V5.14 A52422Recalls & reported problems
Life Technologies Holdings Pte. Ltd. · SW Installer · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- Feb 7, 2024Class IIOpen, Classified
Torrent 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, configurations, software, or data on the instrument
Z-1426-2024 · Root cause: Software design · Recall details · FDA record ↗
Other High throughput DNA sequence analyzer devices
- NextSeq 550Dx Sequencing System 20005715Illumina, Inc. · High Throughput Dna Sequence Analyzer4 recalls3 reports
- MiSeqDx Instrument 15036706Illumina, Inc. · High Throughput Dna Sequence Analyzer2 recalls1 report
- NovaSeq™ 6000Dx 20068232Illumina, Inc. · High Throughput Dna Sequence Analyzer1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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