FDA Device recall Z-0274-2018
QIAamp DSP Virus Kit Cat
- FDA Device
- Class II
- terminated
- Published 2017-12-27
On 2017-12-27 the FDA classified a Class II recall of QIAamp DSP Virus Kit Cat by Qiagen, citing certain lots of the QIAamp DSP Virus Kit, REF 60704, used in analytic workflows could result in decreased performance.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0274-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-07-22 |
| Published | 2017-12-27 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Qiagen |
| Distribution | AR, DE, IN |
Product
QIAamp DSP Virus Kit Cat. No. 60704
Reason
Certain lots of the QIAamp DSP Virus Kit, REF 60704, used in analytic workflows could result in decreased performance.
Identifiers
| code_info | QIAamp DSP Virus Kit, Cat. No. 60704, lot 154025928 , 154027751, 154029053, 154029743 and 154029744. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
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FDA Device · Class II · 2018-08-08 · Qiagen
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0274-2018%22
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