Device recall
Z-1751-2010: PLAC Test Reagent Kit, immuno-turbidimetric method, Part Number 90115, Beckman…
FDA device recall · Class II · DiaDexus, Inc
Key facts
| Recall number (Z-number) | Z-1751-2010 |
|---|---|
| Recall event | 53856 |
| Product | PLAC Test Reagent Kit, immuno-turbidimetric method, Part Number 90115, Beckman test kit, manufactured by DiaDexus, South San Francisco, CA. |
| Product code | NOE |
| Recalling firm | DiaDexus, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 26, 2011 |
| 510(k) numbers | K072599 |
| FEI number | 3003643666 |
At a glance
- 1–9 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