Class II — Ab Sciex
| Recalling firm | AB SCIEX |
|---|---|
| Registered facility | AB SCIEX LP (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Software- AB SCIEX API 3200MD LC/MS/MS SYSTEM with MultiQuantMD 3.0 software may provide incorrect data for patient diagnosis |
| 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. |
| Quantity | 6 units |
| Distribution | FL, NC, OK, PA, TX |
| Initiated | 2014-07-15 |
| Classified | 2014-09-08 |
| Terminated | 2014-10-01 |
| Recall number | Z-2609-2014 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Ab Sciex (Z-2609-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/68821/
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