FDA Enforcement Class III Ongoing

Immunoassay Premium Control Tri Level-In vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes Catalog Number: IA2633

Recall: Z-2022-2023 · Reported July 5, 2023

Enforcement

Recall Number
Z-2022-2023
Event ID
92344
Classification
Class III
Status
Ongoing
Product Type
Devices
Firm
Randox Laboratories Ltd.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
July 5, 2023
Initiation Date
May 4, 2023
Classification Date
June 28, 2023
Address
55 Diamond Road, N/A, Crumlin (North), N/A, N/A, Ireland

Description

Immunoassay Premium Control Tri Level-In vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes Catalog Number: IA2633

Reason

Delay in reporting results due to Quality Controls running high outside of range. Target value and range for ACTH in Immunoassay Premium Level 3, IA2640, lot 2031EC and Immunoassay Premium Control Tri Level kit batch 583135 lot 2031EC has been reassigned on the Roche Cobas e801 due to High recovery outside range

Code Info

GTIN: 05055273203837 Batch/Lot Number: 583135 Exp. Date: 28th April 23

Distribution

CA, IL, VA, WA, WI including PR

Quantity

30 kits