QIAGEN recalls EZ1 DSP Virus Kit (48), IVD, REF 62724 intended for in vitro diagnostic use.

Recall date

May 28, 2018

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2596-2018

FDA classification

Class II

Brand / firm

QIAGEN

Sold / distributed

Domestic - MD Internationally - AE, AU , CZ, DE, DZ, ES, FR, GB, HK , IE, IT, NO, RO & SA

Why it was recalled

Underfilled reagent well that could lead to incorrect results

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

What was recalled

EZ1 DSP Virus Kit (48), IVD, REF 62724 intended for in vitro diagnostic use.