Device recall
Z-2609-2014: AB SCIEX API 3200MD" LC/MS/MS System with software: MultiQuantMD 3.0In vitro…
FDA device recall · Class II · Ab Sciex
Key facts
| Recall number (Z-number) | Z-2609-2014 |
|---|---|
| Recall event | 68821 |
| 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. |
| Product code | DOP |
| Recalling firm | Ab Sciex |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 1, 2014 |
| FEI number | 3008935545 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database