FDA Enforcement Class II Ongoing

Alinity c Iron Reagent, Reference Number 08P3920

Recall: Z-0326-2024 · Reported November 29, 2023

Enforcement

Recall Number
Z-0326-2024
Event ID
93298
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Sentinel CH SpA
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
November 29, 2023
Initiation Date
September 29, 2023
Classification Date
November 17, 2023
Address
Via Robert Koch 2, N/A, Milan, N/A, N/A, Italy

Description

Alinity c Iron Reagent, Reference Number 08P3920

Reason

A high recovery of Iron assay has been observed at some customer sites. Internal studies confirmed the positive shift of Quality Control and patient samples results, up to 15% for Iron Products (Alinity c Iron Reagent REF. 08P3920) to be used on Abbott Alinity Instrument and to 30% for Iron Products (IRON REF. 6K95-41 and IRON REF. 6K95- 30) to be used on Abbott Architect Instrument. When using the affected lots, there is a potential for delay in reporting patient results due to QC failure, also a potential for falsely elevated results.

Code Info

UDI-DI: 00380740136253; Lot Number: 21046Y600, 21118Y600, 30227Y600, 30302Y600

Distribution

Worldwide - US Nationwide distribution.

Quantity

4400 kits