Device recall
Z-0240-04: AEROSET/ARCHITECT c8000 Urea Nitrogen Models: 7D75-01; 7D75-20; 7D75-30
FDA device recall · Class II · Abbott Laboratories Diagnostic Div
Key facts
| Recall number (Z-number) | Z-0240-04 |
|---|---|
| Recall event | 27822 |
| Product | AEROSET/ARCHITECT c8000 Urea Nitrogen Models: 7D75-01; 7D75-20; 7D75-30 |
| Product code | CDQ |
| Recalling firm | Abbott Laboratories Diagnostic Div |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 25, 2012 |
| FEI number | 2018433 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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