AB SCIEX API 3200MD" LC/MS/MS System with software: MultiQuantMD 3 — Class II medical device recall Z-2609-2014
Terminated recall by Ab Sciex, reported 2014-09-17, distributed in FL, NC, OK, PA, TX. Software- AB SCIEX API 3200MD LC/MS/MS SYSTEM with MultiQuantMD 3.0 software may provide incorrect data for pa
| Recall number | Z-2609-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ab Sciex, Framingham, MA, United States |
| Recall initiated | 2014-07-15 |
| Classified | 2014-09-08 |
| Reported by FDA | 2014-09-17 |
| Terminated | 2014-10-01 |
| Distributed | FL, NC, OK, PA, TX |
| Quantity | 6 units |
| Reason classes | software |
| Serial numbers | BV20031308, BV20051310, BV20071311, BV20081311, BV20101401, BV20131401 |
| Model numbers | 5024543 |
Product
AB SCIEX API 3200MD" LC/MS/MS System with software: MultiQuantMD 3.0In vitro diagnostic to identify inorganic or organic compounds (e.g., lead, mercury, and drugs) in human specimens Part Number 5024543.
Reason for recall
Software- AB SCIEX API 3200MD LC/MS/MS SYSTEM with MultiQuantMD 3.0 software may provide incorrect data for patient diagnosis
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-2609-2014. 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.