Cliquid MD version 3 — Class II medical device recall Z-0175-2022
Terminated recall by AB SCIEX, reported 2021-11-03, distributed nationwide. The values of the Internal Standard (IS) concentrations are incorrectly derived when the user builds a customi
| Recall number | Z-0175-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | AB SCIEX, Concord, N/A, Canada |
| Recall initiated | 2021-10-04 |
| Classified | 2021-10-26 |
| Reported by FDA | 2021-11-03 |
| Terminated | 2024-01-23 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, CH, DE, ES, FI, FR, GB, HK, IT, JP, NO |
| Quantity | 30 |
| Model numbers | 5088288 |
Product
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
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0175-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.