Medical device recalls Moderate risk

Qiagen, GmbH recalls QIAamp DSP Virus Kit Cat. No. 60704

Recall date
July 22, 2017
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0274-2018
FDA classification
Class II
Brand / firm
Qiagen, GmbH
Sold / distributed
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

Why it was recalled

Certain lots of the QIAamp DSP Virus Kit, REF 60704, used in analytic workflows could result in decreased performance.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

QIAamp DSP Virus Kit Cat. No. 60704

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