Class II — Qiagen, GmbH
| Recalling firm | QIAGEN, GmbH |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Certain lots of the QIAamp DSP Virus Kit, REF 60704, used in analytic workflows could result in decreased performance. |
| Product | QIAamp DSP Virus Kit Cat. No. 60704 |
| Quantity | 555 |
| Distribution | AR; AT; BE; CH; CN; CZ; DE; ES; FR; GB; GR; HK; IN; IR, IT; KR; MX; NL; NP, PH; PK; PL; TR, TW; US; UY, VN |
| Initiated | 2017-07-22 |
| Classified | 2017-12-21 |
| Terminated | 2018-07-26 |
| Recall number | Z-0274-2018 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Qiagen, GmbH (Z-0274-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/78646/
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