PlainRecalls
FDA Devices Moderate Class II Terminated

QIAamp DSP Virus Kit Cat. No. 60704

Reported: December 27, 2017 Initiated: July 22, 2017 #Z-0274-2018

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.

Details

Recalling Firm
Qiagen, GmbH
Units Affected
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
Location
Hilden

Frequently Asked Questions

What product was recalled?
QIAamp DSP Virus Kit Cat. No. 60704. Recalled by Qiagen, GmbH. Units affected: 555.
Why was this product recalled?
Certain lots of the QIAamp DSP Virus Kit, REF 60704, used in analytic workflows could result in decreased performance.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 27, 2017. Severity: Moderate. Recall number: Z-0274-2018.