Device recall
Z-0769-04: Clinical Chemistry Uric Acid; LN 7D76-20
FDA device recall · Class II · Abbott Laboratories Diagnostic Div
Key facts
| Recall number (Z-number) | Z-0769-04 |
|---|---|
| Recall event | 28627 |
| Product | Clinical Chemistry Uric Acid; LN 7D76-20 |
| Product code | CDO |
| Recalling firm | Abbott Laboratories Diagnostic Div |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 10, 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