RecallRadar

FDA Device recall Z-0188-2020

Torrent Suite Dx Software Version 5.8 Catalog Number:A36601 and A36602 OEM Customer software: Torrent Suite Dx T430 Software v5.0 DARUI DR-…

On 2019-10-30 the FDA classified a Class II recall of Torrent Suite Dx Software Version 5.8 Catalog Number:A36601 and A36602 OEM Customer software: Torrent Suite Dx T430 Software v5.0 DARUI DR-… by Life Technologies Holdings Pte, citing torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx Instrument System, incorrectly displays a positive result when a different analytical or de novo variant is det….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0188-2020
ClassificationClass II
Statusterminated
Initiated2019-09-26
Published2019-10-30
Last updated2026-09-13 11:55 UTC
CompanyLife Technologies Holdings Pte
DistributionAZ, CA, CO, CT, FL, GA, IN, MA, MD, NC, NJ, NM, NY, OR, TX, VA, WA

Product

Torrent Suite Dx Software Version 5.8 Catalog Number:A36601 and A36602 OEM Customer software: Torrent Suite Dx T430 Software v5.0 DARUI DR-SEQ 800 Software UDI:(01)10190302014090 (11)000000(10)5.8 (240)A36601

Reason

Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx Instrument System, incorrectly displays a positive result when a different analytical or de novo variant is detected at the same locus as a specified clinical variant

Identifiers

code_infoThe field action is associated with the software available on the PGM Dx instrument, therefore no lot code is applicable for this part type

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0188-2020%22

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