QIAamp DSP Virus Kit Cat — Class II medical device recall Z-0274-2018
Terminated recall by Qiagen, GmbH, reported 2017-12-27, distributed in AR. Certain lots of the QIAamp DSP Virus Kit, REF 60704, used in analytic workflows could result in decreased perf
| Recall number | Z-0274-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Qiagen, GmbH, Hilden, Germany |
| Recall initiated | 2017-07-22 |
| Classified | 2017-12-21 |
| Reported by FDA | 2017-12-27 |
| Terminated | 2018-07-26 |
| Distributed | AR |
| Quantity | 555 |
| Lot numbers | 154025928, 154027751, 154029053, 154029743, 154029744 |
| Model numbers | 60704 |
Product
QIAamp DSP Virus Kit Cat. No. 60704
Reason for recall
Certain lots of the QIAamp DSP Virus Kit, REF 60704, used in analytic workflows could result in decreased performance.
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-0274-2018. 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.