Recall Z-0283-2020

Randox Laboratories Ltd. · initiated August 9, 2019

Class II Terminated

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

Liquid Protein Calibrators (SP CAL (LIQ)) Catalogue Number: IT2691 GTIN: 05055273204032 Product Usage: Liquid Protein Calibrators are intended for in vitro diagnostic use in the calibration of ASO, Complement C3, Complement C4, CRP, Ferritin, Haptoglobin, IgA, IgG, IgM, Prealbumin, and Transferrin assays on Clinical Chemistry and Immunoassay systems, Abbott Spectrum, Abbott Aeroset, Abbott Architect i2000, Architect i2000sr, Ace analyser, Bayer Advia 1650, Advia 2400, Advia 1200, Dade Dimension RXL, Dimension AR, Hitachi 704, Hitachi 717, Hitachi 911, Hitachi 917, Hitachi 912, Hitachi 747, Kone progress, AU800, AU600, AU400, AU2700, AU5400, Selectra Vitalab, Synchron CX4, Synchron CX5, Synchron CX7, Synchron LX20, ILAB300, ILAB900, ILAB1800, ILAB600, RX Daytona, RX Imola, Cobas Mira, Cobas Mira S, Cobas Mira Plus systems

Codes / lots: Batch/Lot # 440973 /1748 1752IT 451414 /1748 1752IT 470531 /1813 1817IT 480859 /1813 1817IT

Reason for recall

The assigned value for Rheumatoid Factor over recovers against the reference material RF serum, 1st British standard from NIBSC. Ref = 64/002. The calibrator values have been adjusted to re-align to the reference material.

FDA-determined cause: Nonconforming Material/Component

Action taken

1. Review your reagent inventory and replace the value sheet with the new values provided. 2. Review results generated with the affected batches in line with the clinical profile of the patient. 3. Discuss the contents of this notice with your Medical Director. 4. Complete and return the response form 12187-QA to teclhnical.services@randox.com within five working days.

Details

Recall number
Z-0283-2020
Initiated
August 9, 2019
Terminated
January 8, 2021
Product code
JIX – Calibrator, Multi-Analyte Mixture
Quantity
100 kits
Distribution
US Nationwide distribution in the states of WV, ME, NJ, CA, and Puerto Rico.
Recalling firm
Randox Laboratories Ltd., Crumlin, North

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-0282-2020 Class IIRheumatoid Factor Standard (RF CAL) Catalogue Number: RF2301 GTIN: 05055273205039…The assigned value for Rheumatoid Factor over recovers against the reference material RF serum, 1st British… 08/09/2019Terminated