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
- 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