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Recall Observatory FDA recall evidence

Device product

ABL90 FLEX, model no. 393-090; and Spare Part Hemolyzer Units (902-980): R0526 - R0941 - Product Usage: are intended for use by trained technologists, nurses, physicians and therapists. It is intended for use in a laboratory environment, near patient or point-of-care setting.

Z-2139-2020

November 21, 2019

Class II

Product summary

Firm
Radiometer Medical ApS
Event
Event 85390
Status
Terminated
Classification
Class II
Quantity
1233 units
Official record key
device-enforcement:Z-2139-2020

Official wording

Reason: The analyzers fail on S7950 (Range +) QC measurements due to the hemolyzer cuvettes, a subcomponent of the optical system which measures ctHb and derivates. In a cuvette with light shunt, some of the received light has not been transmitted through the sample. This will lead to a perturbed and non-linear absorbance spectrum which results in measurement errors.

Code information: ABL90 FLEX Model no. 393-090: R0659 - R0977 and Spare Part Hemolyzer Units (902-980): R0526 - R0941

Distribution pattern: Worldwide distribution - US Nationwide. Also distributed OUS.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The analyzers fail on S7950 (Range +) QC measurements due to the hemolyzer cuvettes, a subcomponent of the optical system which measures ctHb and derivates. In a cuvette with light shunt, some of the received light has not been transmitted through the sample. This will lead to a perturbed and non-linear absorbance spectrum which results in measurement errors.