FDA Enforcement Class II Terminated

IM Abbott Alinity ci-series (abdicqii) accessory driver v8.00.0001 software product that can receive information from a hospital computer system (also called a Laboratory Information System [LIS]).

Recall: Z-0203-2019 · Reported October 31, 2018

Enforcement

Recall Number
Z-0203-2019
Event ID
81005
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Data Innovations, LLC
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
October 31, 2018
Initiation Date
August 29, 2018
Classification Date
October 22, 2018
Termination Date
February 5, 2019
Address
120 Kimball Ave Ste 100, N/A, South Burlington, VT, 05403-6837, United States

Description

IM Abbott Alinity ci-series (abdicqii) accessory driver v8.00.0001 software product that can receive information from a hospital computer system (also called a Laboratory Information System [LIS]).

Reason

Quality control results are not processed for Abbott Diagnostics Alinity ci series (abdicqii) instrument. This has been determined to be a driver malfunction. When an instrument transmits results from a quality control (QC) sample ID ("Q^Control" in SPM segment), and the option Hold Results Until Complete is enabled, the results do not parse into IM. The communication Trace shows the sample being transmitted, but no information is logged in the Specimen Event Log (SEL). There is a potential for harm if QC results are not processed, downstream auto verification rules may misfire based on missing QC results leading to a delay in, or incorrect treatment. QC results will not be available for evaluation by the lab. There have been no reported instances of patient harm from this malfunction.

Code Info

accessory driver version number 8.00.0001

Distribution

Distributed to OK. Foreign distribution to Argentina, Hong Kong, Malaysia, Thailand, Germany, Jordan, Australia, and Switzerland.

Quantity

9