Medical device recalls Moderate risk

RANDOX LABORATORIES, LTD. recalls Randox Lipase Assay: Lipase Colorimetric Reagent - Product Usage: A Lipase test system is a device intended for the qua…

Recall date
June 26, 2020
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2751-2020
FDA classification
Class II
Brand / firm
RANDOX LABORATORIES, LTD.
Sold / distributed
Worldwide distribution - US Nationwide distribution including in the states of Puerto Rico and WV.

Why it was recalled

Randox have confirmed imprecision of quality control and patient samples when using specific Randox Lipase reagent batches.

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

What was recalled

Randox Lipase Assay: Lipase Colorimetric Reagent - Product Usage: A Lipase test system is a device intended for the quantitative in vitro determination of Lipase in human serum and plasma.

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