Alinity m Integrated Reaction Units (IRU)
FDA Recall Z-0710-2022 · Posted None
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Recalling FirmAbbott Molecular, Inc.
Recall StatusTerminated
Product CodeOOI
Date Initiated2022-02-11
Date Terminated2023-04-14
Product Quantity3063 kits
Reason for Recall
There is potential for the Reaction Vessels (RVs) detaching from the RV cap during transport by the pipettor robot.
Firm 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.
Root Cause
Under Investigation by firm
Distribution Pattern
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.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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