Device recall
Z-2501-2010: UCG Beta Slide Monoclonal II is a latex agglutination inhibition slide test for…
FDA device recall · Class III · Inverness Medical Professional Diagnostics
Key facts
| Recall number (Z-number) | Z-2501-2010 |
|---|---|
| Recall event | 54745 |
| Product | UCG Beta Slide Monoclonal II is a latex agglutination inhibition slide test for the detection of hCG in urine. This test is used for the diagnosis of pregnancy. |
| Product code | LCX |
| Recalling firm | Inverness Medical Professional Diagnostics |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 14, 2012 |
| FEI number | 3003764480 |
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