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Recall Observatory FDA recall evidence

Device product

AggreGuide A-100 Instrument

Z-1639-2022

July 23, 2019

Class II

Product summary

Firm
Aggredyne, Inc.
Event
Event 90588
Status
Completed
Classification
Class II
Quantity
47
Official record key
device-enforcement:Z-1639-2022

Official wording

Reason: The firm identified a software design issue where the improper shut down of the instrument resulted in speeds.csv file contents of the software version 5.1 being erased. Due to this issue, the target RPM for the assay is 0 and the motor output required to achieve this RPM is also 0. Therefore, when the assay is run, the software applies 0 Volts to the motor and performs a 0 RPM assay. Because of this, there is no mixing of the blood with agonist and no moving of aggregates happens in front of the optical detectors. The resulting PAI is 0 and the result is displayed as Low.

Code information: UDI-DI: 00856893004065; Software Versions 5.1 or 5.2; Serial Numbers Between xx0001 and xx0160

Distribution pattern: International distribution to the country of South Korea.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software design issue