FDA Recall Terminated

Alinity m Integrated Reaction Units (IRU)

Recall: Z-0710-2022 · Initiated February 11, 2022

Recall

Recall Number
Z-0710-2022
Event Number
89603
Firm
Abbott Molecular, Inc.
FEI Number
3005248192
Product Code
OOI
Status
Terminated
Root Cause
Under Investigation by firm
Initiated
February 11, 2022
Terminated
April 14, 2023
Address
1300 E Touhy Ave, Des Plaines, IL, 60018-3315

Description

Alinity m Integrated Reaction Units (IRU)

Reason

There is potential for the Reaction Vessels (RVs) detaching from the RV cap during transport by the pipettor robot.

Action

On February 11, 2022, Abbott Molecular issued a Product Recall letter to all customers who received Integrated Reaction Unit (IRU) List Number 09N26-010 Lot Numbers 766233, 770433, 771200, 771201, and 773642 used with the Alinity m System. Consignees must complete and return the included customer reply form. Customers are instructed to follow the Necessary Actions outlined in the Customer Letter: Discontinue use of and discard all remaining inventory of IRU Lots 766233, 770433, 771200, 771201, and 773642. To coordinate replacement, contact your local Molecular Diagnostics at Abbott representative. If RVs are found inside the instrument with no cap and there are associated 1998 errors, please contact an Abbott representative to inspect the instrument. Results generated between the onset of the associated 1998 errors and the identification of the RV with no cap inside the instrument should be considered presumptive. Retesting of samples that yielded positive results during this timeframe should be considered.

Distribution

US Nationwide distribution in the states of AZ, CA, CO, CT, DC, FL, GA, IL, KY, LA, MA, MI, MO, NC, NJ, NY, OK, RI, SD, TX, WA, and WI.

Quantity

3063 kits