Life Technologies Corporation: Medical Device Recall in 2024 - (Recall #: Z-1426-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Torrent Suite Dx Software versions 5.14 and earlier used in connection with Ion PGM DX Systems-IVD intended for targeted sequencing of human genomic DNA (gDNA) from peripheral whole-blood samples and DNA and RNA extracted from formalin-fixed, paraffin-embedded (FFPE) samples. The Ion PGM Dx Instrument System is not intended for whole genome or de novo sequencing Product Name Installer /SKU /Updater SKU: (1) Torrent Suite Dx Software 5.14 -A52422/ A52417 (2) Torrent Suite Dx Software 5.12.5- A46166/ A46167 (3)Torrent Suite Dx Software 5.8- A36601/ A36602 (4)Torrent Suite Dx Software 5.6.4- A33178/ A33178 (5)Torrent Suite Dx Software 5.0- A29166/ A29166

Product Classification:

Class II

Date Initiated: February 7, 2024

Date Posted: April 10, 2024

Recall Number: Z-1426-2024

Event ID: 94122

Reason for Recall:

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

Status: Ongoing

Product Quantity: 28 units

Code Information:

UDI: 10190302017848;10190302016810 Torrent Suite Dx Software versions 5.14 and earlier

Distribution Pattern:

US Nationwide distribution in the states of CA, IN, NC OR, TN.

Voluntary or Mandated:

Voluntary: Firm initiated