PlainRecalls
FDA Devices Moderate Class II Ongoing

Microalbumin Calibrator Series (mALB CAL)-IVD to calibrate the Microalbumin Assay Catalog Number: MA2426

Reported: April 24, 2024 Initiated: January 31, 2024 #Z-1594-2024

Product Description

Microalbumin Calibrator Series (mALB CAL)-IVD to calibrate the Microalbumin Assay Catalog Number: MA2426

Reason for Recall

Microalbumin Calibrator Series, MA1567 & MA2426, is running with a negative bias compared to other method may misclassify patient results. Users may experience a shift in Quality Control and patient sample recovery of up to +12%.

Details

Recalling Firm
Randox Laboratories Ltd.
Units Affected
6 units
Distribution
US Nationwide distribution in the states of GA, MA, WV including PR.
Location
Crumlin (North)

Frequently Asked Questions

What product was recalled?
Microalbumin Calibrator Series (mALB CAL)-IVD to calibrate the Microalbumin Assay Catalog Number: MA2426. Recalled by Randox Laboratories Ltd.. Units affected: 6 units.
Why was this product recalled?
Microalbumin Calibrator Series, MA1567 & MA2426, is running with a negative bias compared to other method may misclassify patient results. Users may experience a shift in Quality Control and patient sample recovery of up to +12%.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 24, 2024. Severity: Moderate. Recall number: Z-1594-2024.