Medical device recalls

Randox Laboratories Ltd. recalls Immunoassay Premium Controls, Model Numbers IA2633 and IA2638 Product Usage: This product is intended for in vitro diag…

Recall date
February 7, 2019
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1105-2019
FDA classification
Class III
Brand / firm
Randox Laboratories Ltd.
Sold / distributed
The products were distributed to the following US states: WV and Puerto Rico.

Why it was recalled

The target value for uptake is incorrect on the value sheet for an analyzer. The target value for this analyzer is listed as 43.8%U and should be 39.4%U.

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

Immunoassay Premium Controls, Model Numbers IA2633 and IA2638 Product Usage: This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes listed in the package insert

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