Recalls for Radioimmunoassay, Angiotensin I And Renin

The recall was initiated because Beckman Coulter has confirmed that the Active Renin IRMA Test Kit may exhibit a decrease in stability of the coated tubes. As a result, quality control and patient sample results may be falsely elevated by up to 72%.

The kit control provided with the GammaCoat Plasma Renin Activity kit was labeled with the incorrect range.

Incorrect calibration standard value may result in 25% higher assay values for controls and patient samples

Incorrect calibration standard value may result in 25% higher assay values for controls and patient samples