Drug recall
Cliquid MD version 3.4 software used in conjunction with Analyst MD software on SCIEX Citrine & 4500MD series…
FDA recall event 88748 · Class II · AB SCIEX
Key facts
| Event ID | 88748 |
|---|---|
| Recall numbers | Z-0175-2022 |
| Recalling firm | AB SCIEX |
| Product type | Devices |
| Products | 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 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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… |
| Initiation date | Oct 4, 2021 |
| Report date | Nov 3, 2021 |
| Termination date | Jan 23, 2024 |
| City | Concord |
| Country | Canada |
| FEI number | 3008336863 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: