Device recall
Z-0222-2007: NOW Legionella Urinary Antigen Test. 22 test kit. For In Vitro Diagnostic Use…
FDA device recall · Class II · Inverness Medical Professional Diagnostics
Key facts
| Recall number (Z-number) | Z-0222-2007 |
|---|---|
| Recall event | 36699 |
| Product | NOW Legionella Urinary Antigen Test. 22 test kit. For In Vitro Diagnostic Use Product Code: 852-000 |
| Product code | MJH |
| Recalling firm | Inverness Medical Professional Diagnostics |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 13, 2007 |
| 510(k) numbers | K982238 |
| FEI number | 1221359 |
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