ClearanceBrief
Recall Z-1639-2022 ยท JOZ System, Automated Platelet Aggregation

Aggredyne, Inc.

AggreGuide A-100 Instrument

DateJul 23, 2019
StatusCompleted
ReasonThe 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.
Root causeSoftware design
ActionOn 7/23/2019, a Service Bulletin was sent to distributors and users informing them to follow the User Manual, which states: 1) To shut down the instrument: Press the Shut Down button and wait. 2) Continue to wait for the screen message stating that it is safe to turn off your computer (this may take 15 seconds or more). 3) Turn off power switch only after the message "It is now safe to turn off your computer" is displayed. 4) A future communication from the recalling firm will be provided when the software update is available. On 7/8/22 updated Service Bulletin was sent to the distributor not
Quantity47
DistributionInternational distribution to the country of South Korea.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K122162AGGREGUIDE
Aggredyne, Inc., Dec 20, 2013
K163274AggreGuide A-100 AA Assay, AggreGuide A-100 Instrument
Aggredyne, Inc., Apr 5, 2017
K181777AggreGuide A-100 ADP
Aggredyne, Inc., Mar 29, 2019