AB SCIEX: Medical Device Recall in 2021 - (Recall #: Z-0175-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Cliquid MD version 3.4 software used in conjunction with Analyst MD software on SCIEX Citrine & 4500MD series liquid chromatography-tandem mass spectrometry (LC-MS/MS) systems. Model No. 5088288

Product Classification:

Class II

Date Initiated: October 4, 2021

Date Posted: November 3, 2021

Recall Number: Z-0175-2022

Event ID: 88748

Reason for Recall:

The values of the Internal Standard (IS) concentrations are incorrectly derived when the user builds a customized test, then set the IS column to hidden and left the column empty. This may lead to the user making incorrect conclusions using incorrect results.

Status: Terminated

Product Quantity: 30

Code Information:

Software version 3.4

Distribution Pattern:

Worldwide distribution - US Nationwide distribution in the states of District of Columbia, Florida, Illinois, Louisiana, Maryland, Michigan, Missouri, New Jersey, New York, North Carolina, Ohio, Pennsylvania, Tennessee, Utah, Wisconsin and the countries of Austria, Finland, Germany, Hong Kong, Italy, Japan, Norway, Spain, Switzerland, United Kingdom, Italy, France, and Japan.

Voluntary or Mandated:

Voluntary: Firm initiated