FDAJune 14, 2024device

Discrete photometric chemistry analyzer for clinical use.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Beckman Coulter, Inc. has identified a rise in reagent carousel motion errors in Access 2 Immunoassay System Analyzers that appear to be caused by misaligned index wheels housed within the reagent carousel module. Customers affected by this issue may observe an increase in reagent carousel motion errors or QSMC errors that occur while unloading or loading reagent packs during system initialization and sample processing, which causes a non-operational system status and cancels tests; and patient results may be delayed if these errors cancel test processing.

What to do

FDA enforcement status: Ongoing

Brands named

beckman coulterbeckman

UPCs

574447574494574456574504574470574509

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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