Device recall
Z-1586-2016: Analyst MD Version 1.6.1 and 1.6.2 Software used with the following instruments…
FDA device recall · Class II · Ab Sciex
Key facts
| Recall number (Z-number) | Z-1586-2016 |
|---|---|
| Recall event | 73433 |
| Product | Analyst MD Version 1.6.1 and 1.6.2 Software used with the following instruments: API 3200MD" LC/MS/MS System, Instrument Part Number: 5024501; 3200MD QTRAP LC/MS/MS System, Instrument Part Number: 5024500; Triple Quad" 4500MD LC/MS/MS System, Instrument Part Number: 5031257; QTRAP 4500MD LC/MS/MS… |
| Product code | DOP |
| Recalling firm | Ab Sciex |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 6, 2017 |
| 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