Ion Torrent Dx No Template Control Kit- IVD for detection of DNA and… — Class II medical device recall Z-1707-2020
Terminated recall by Life Technologies Corporation, reported 2020-04-22, distributed nationwide. Extended Expiration Date prior to clearance
| Recall number | Z-1707-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Life Technologies Corporation, Frederick, MD, United States |
| Recall initiated | 2020-03-16 |
| Classified | 2020-04-14 |
| Reported by FDA | 2020-04-22 |
| Terminated | 2021-03-26 |
| Distributed | Nationwide (US) |
| Quantity | 79 units |
| UPC / GTIN / UDI-DI | 10190302006156 |
| Model numbers | A32444 |
Product
Ion Torrent Dx No Template Control Kit- IVD for detection of DNA and RNA isolated from non-small cell lung cancer (NSCLC) tumor specimens Catalog Number: A32444
Reason for recall
Extended Expiration Date prior to clearance
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1707-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.