Z-0274-2018 Class II Terminated

Recalled by Qiagen, GmbH — Hilden

FDA device recall Z-0274-2018 was initiated by Qiagen, GmbH on July 22, 2017 and is designated Class II. Reason for recall: Certain lots of the QIAamp DSP Virus Kit, REF 60704, used in analytic workflows could result in decreased performance. The recall status is terminated (terminated July 26, 2018). Affected quantity: 555.

Recall Details

Product Type
Devices
Report Date
December 27, 2017
Initiation Date
July 22, 2017
Termination Date
July 26, 2018
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
555

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.

Distribution Pattern

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

Code Information

QIAamp DSP Virus Kit, Cat. No. 60704, lot 154025928 , 154027751, 154029053, 154029743 and 154029744.