FDA recall record

Randox Liquid Protein Calibrators-SP CAL-(LIQ)-In vitro diagnostic product used for the recall — FDA Z-2448-2023

As part of the firm's ongoing quality monitoring (see internal complaint # OCC72574), Randox Laboratories have restandardized Ferritin in Liquid Protein…

Class IIclassification
Z-2448-2023official record ID
Aug 30, 2023report date

Recall record at a glance

Official recordZ-2448-2023
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmRandox Laboratories Ltd.
Report dateAug 30, 2023
Recall initiation dateJul 19, 2023
Quantity166 units
LocationCrumlin (North), N/A, Ireland

Official product description

Randox Liquid Protein Calibrators-SP CAL-(LIQ)-In vitro diagnostic product used for the calibration of ASO, Complement C3, Complement C4, CRP, Ferritin, Haptoglobin, IgM, Prealbumin, RF and Transferrin assays Catalogue Number: IT2691

Why the product was recalled

As part of the firm's ongoing quality monitoring (see internal complaint # OCC72574), Randox Laboratories have restandardized Ferritin in Liquid Protein Calibrators, IT2691, to reference material NISBC 19/118. The calibrators lots 2112IT-2116IT, packed into batches 627222, 627224, 634886 and 634887 have been reassigned as part of the restandardization. Following this restandardization, Ferritin results for Quality Control material and patient samples recovered erroneously higher than the targeted calibrator values by approximately +10% across the assay range following.

Distribution information

CA, FL, IL, ME, MI, NC, OH, PA,NJ,

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

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