Recall Z-0274-2018— Qiagen, GmbH
Class II · Terminated
Class II FDA medical device recall by Qiagen, GmbH, initiated 2017-07-22, terminated 2018-07-26. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Qiagen, GmbH
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-07-22
- Terminated
- 2018-07-26
- Firm location
- Hilden, Germany
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.