Device recall
Z-2432-2008: Xpect Giardia/Cryptosporidium Kit, Ref 24050520, 20 tests per kit, For In Vitro…
FDA device recall · Class II · Remel, Inc
Key facts
| Recall number (Z-number) | Z-2432-2008 |
|---|---|
| Recall event | 49090 |
| Product | Xpect Giardia/Cryptosporidium Kit, Ref 24050520, 20 tests per kit, For In Vitro Diagnostic Use. A rapid test for the direct qualitative detection of Giardia and Cryptosporidium antigens in fecal specimens. |
| Product code | MHI |
| Recalling firm | Remel, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 21, 2010 |
| 510(k) numbers | K031834 |
| FEI number | 1924669 |
At a glance
- 1–9 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