Life Technologies Corporation recalls
Every recall we track for Life Technologies Corporation — 12 in all, from 2017–2024 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Life Technologies Corporation peaked in 2020 (6); 12 since 2017.
All FDA recall records for Life Technologies Corporation since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 1 | 0 | 1 |
| 2018 | 0 | 0 | 2 | 0 | 2 |
| 2019 | 0 | 0 | 0 | 2 | 2 |
| 2020 | 0 | 0 | 6 | 0 | 6 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 1 | 0 | 0 | 1 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for Life Technologies Corporation recalls
What to do if you have a recalled Life Technologies Corporation product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Life Technologies Corporation recalls
7 shown- Use cautionMedical device
Life Technologies Corporation recalls Torrent Suite Dx Software versions 5.14 and earlier used in connection with Ion PGM DX Systems-IVD intended for
Life Technologies recalls Torrent Suite Dx Software versions 5.14 and earlier for Ion PGM DX Systems. Exploitation could allow attackers to alter settings, configurations, or data on the instrument.
Life TechnologiesFeb 7, 2024 - Lower riskMedical device
Life Technologies Corporation recalls The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19 Interpretive Software v2.0 or v2.2 (used with the
Life Technologies recalls specific versions of their COVID-19 test software due to potential false negatives and false positives, which could lead to inaccurate test results and increased retesting.
Life TechnologiesAug 6, 2020 - Lower riskMedical device
Life Technologies Corporation recalls Oncomine Dx Target Test DNA Control-IVD for detection of DNA and RNA isolated from non-small cell lung cancer (NSCLC)
Life Technologies recalls Oncomine Dx Target Test DNA Control-IVD for NSCLC detection due to extended expiration date prior to clearance. Affected lots may expire before intended use.
Life TechnologiesMar 16, 2020 - UnratedMedical device
Life Technologies Corporation recalls StemPro¿ MSC SFM CTS"
Life Technologies recalls StemPro MSC SFM CTS devices with specific lot numbers due to untested supplier components. Affected units may have adventitious agents that could pose health risks.
Life TechnologiesJun 11, 2019 - Lower riskMedical device
Life Technologies Corporation recalls Oncomine Dx Target Test, (Model No. A32451), Oncomine Dx Target RNA/DNA Panel (Model No. A32441). A qualitative In
Life Technologies recalls two cancer test kits due to potential false negatives in ROS1 fusion detection, which could lead to incorrect treatment decisions.
Life TechnologiesFeb 8, 2018 - Lower riskMedical device
Life Technologies Corporation recalls Human Fetal Hemoglobin (HBF-1) FITC Conjugate
Life Technologies recalls three lots of Human Fetal Hemoglobin FITC Conjugate due to potential false positives in tests. Affected units may cause incorrect results in patient samples and controls.
Life TechnologiesFeb 7, 2018 - Lower riskMedical device
Life Technologies Corporation recalls Oncomine Dx Target Test User Guides and Assay Definition File, Model: A32461; UDI:
Life Technologies recalls Oncomine Dx Target Test User Guides and Assay Definition Files for non-small cell lung cancer tests. These may report incorrect results when used on samples other than NSCLC tumors.
Life TechnologiesDec 4, 2017
Life Technologies Corporation recall questions
How many recalls has Life Technologies Corporation had?
12 recalls from Life Technologies Corporation are on record with U.S. safety agencies, from 2017–2024.
What is the most recent Life Technologies Corporation recall?
Life Technologies Corporation recalls Torrent Suite Dx Software versions 5.14 and earlier used in connection with Ion PGM DX Systems-IVD intended for, dated Feb 7, 2024. Every Life Technologies Corporation recall is listed on this page, newest first.
Why are Life Technologies Corporation products recalled?
The most common reasons on record: Extended Expiration Date prior to clearance (4); Component was not tested by the supplier for adventitious agents (2).
What should I do if I have a recalled Life Technologies Corporation product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Life Technologies Corporation recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.