Device recall
Z-0472-06: Uritek TC-101Urine Analyzer, catalog number TC-101
FDA device recall · Class II · Teco Diagnostics
Key facts
| Recall number (Z-number) | Z-0472-06 |
|---|---|
| Recall event | 34304 |
| Product | Uritek TC-101Urine Analyzer, catalog number TC-101 |
| Product code | KQO |
| Recalling firm | Teco Diagnostics |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 7, 2012 |
| FEI number | 1832216 |
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