Z-0668-2019 Class II Terminated

Recalled by Abbott Ireland Diagnostics Division — Co. Longford

Recall Details

Product Type
Devices
Report Date
January 2, 2019
Initiation Date
November 21, 2018
Termination Date
April 1, 2021
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
157 units

Product Description

Alinity i Progesterone Reagent Kit, List Number 08P3620

Reason for Recall

Abbott has become aware of a manufacturing issue that can result in damage to a bottle neck in some of the reagent cartridges found in the lots listed in Appendix A. If a bottle neck is damaged, it may cause a failure during the reagent loading process on the Alinity i instrument.

Distribution Pattern

AR, FL, GA, MD, OK, VA

Code Information

UDI/Lot Numbers (01)00380740121877 (17)190503(10) 91254UI00 / 91254UI00 (01)00380740121877 (17)190618(10)92360UI00 / 92360UI00