FDAApril 30, 2025device

Sample probe sucks a sample dispensed into a tube or cup and discharges the appropriate amount into a cuvette. Lot 178713114 - 179433670

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

The hazard

Sample probes with defective probe tips, when used with clinical chemistry analyzers, may lead to a lower concentration being dispensed, which may not be detectable by QC checks, which could lead to the reporting of false low test results (Max 34% error at 1.0 microliters and 7% error at 1.6 microliters sample dispensing volume), which may lead to delayed recognition and treatment.

What to do

FDA enforcement status: Completed

Brands named

beckman coulter mishima k kbeckmanbeckman coulter

UPCs

149876665407321498766654068814987666540701149876665407251498766654298914987666542996149876665430091498766654330614987666543313150995903462491498766653530114987666535318

Recall history

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

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