Device recall
Z-2526-2016: AB Sciex API 3200MD" LC/MS/MS System. In-Vitro Diagnostic Instrument Part Number…
FDA device recall · Class II · Ab Sciex
Key facts
| Recall number (Z-number) | Z-2526-2016 |
|---|---|
| Recall event | 74520 |
| Product | AB Sciex API 3200MD" LC/MS/MS System. In-Vitro Diagnostic Instrument Part Number (REF): 5024501 3200MD series and 4500MD series are mass spectrometers intended to identify inorganic or organic compounds (e.g., lead, mercury, and drugs) in human specimens by ionizing the compound under investigation… |
| Product code | DOP |
| Recalling firm | Ab Sciex |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 2, 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